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Agenda
Reg Review
ICR
Information Collection List
IC Title
Status
Responses
Hours
Dollars
Document Type
Form No.
Form Name
(Burden Change Due to Rulemaking) Recordkeeping for Electronic Products: General Requirements
Modified
16687
286350
0
(Burden Change Due to Rulemaking) Reporting for Electronic Products: General Requirements
Modified
24
102744
0
Form and Instruction
FDA 3626
Diagnostic X-Ray
Form and Instruction
FDA 3626
Diagnostic X-Ray (esubmitter)
Form and Instruction
FDA 3627
CT X-Ray
Form and Instruction
FDA 3627
CT X-Ray (esubmitter)
Form and Instruction
FDA 3639
Cabinet X-Ray (esubmitter)
Form and Instruction
FDA 3632
Laser
Form and Instruction
FDA 3632
Laser (esubmitter)
Form and Instruction
FDA 3640
Laser Light Show
Form and Instruction
FDA 3640
Laser Light Show (esubmitter)
Form and Instruction
FDA 3630
Sunlamp
Form and Instruction
FDA 3630
Sunlamp (esubmitter)
Form and Instruction
FDA 3646
Mercury vapor lamp (esubmitter)
Form and Instruction
FDA 3644
Ultrasonic therapy (esubmitter)
Form and Instruction
FDA 3659
TV (esubmitter)
Form and Instruction
FDA 3660
Microwave oven (esubmitter)
Form and Instruction
FDA 3801
UV lamps
Form and Instruction
FDA 3629
General abbreviated report (esubmitter)
Form and Instruction
FDA 3661
X-Ray Report (esubmitter)
Form and Instruction
FDA 3662
Cephalometric Report (esubmitter)
Form and Instruction
FDA 3663
Microwave products (non-oven) (esubmitter)
Form and Instruction
FDA 3628
General Med X-ray annual report (esubmitter)
Form and Instruction
FDA 3634
TV annual report (esubmitter)
Form and Instruction
FDA 3638
Diagnostic X-ray annual report (esubmitter)
Form and Instruction
FDA 3641
Cabinet x-ray annual report (esubmitter)
Form and Instruction
FDA 3643
MIcrowave oven annual report
Form and Instruction
FDA 3636
Laser annual report (esubmitter)
Form and Instruction
FDA 3631
Sunlamp annual report (esubmitter)
Form and Instruction
FDA 2579
Report of Assembly of a Diagnostic X-Ray System
Form and Instruction
FDA 2767
Notice of Availability of Sample Electronic Product
Form and Instruction
FDA 2877
Declaration for Imported Electronic Products Subject to Radiation Control Standards
Form and Instruction
FDA 3649
Accidental Radiation Occurrence Report
Form and Instruction
FDA 3649
Accidental Radiation Occurrence Report (esubmitter)
Form and Instruction
FDA 3633
General Variance Request (esubmitter)
Form and Instruction
FDA 3635
Laser Show Notification (esubmitter)
Form and Instruction
FDA 3637
Original Equipment Manufacturer (OEM) Report (esubmitter)
Form and Instruction
FDA 3147
Application for a Variance from 21 CFR 1040.11(c) for a Laser Light Show, Display, or Device
Form and Instruction
FDA 3147
Application for a Variance from 21 CFR 1040.11(c) for a Laser Light Show, Display, or Device (esubmitter)
Form and Instruction
FDA 3642
General Correspondence
Form and Instruction
FDA 3645
Therapy Ultrasound Annual Report
Form and Instruction
FDA 3645
Therapy Ultrasound Annual Report (esubmitter)
Form and Instruction
FDA 3646
Mercury Vapor Lamp Product Report
Form and Instruction
FDA 3647
Mercury Vapor Lamp Annual Report
Form and Instruction
FDA 3647
Mercury Vapor Lamp Annual Report (esubmitter)
Form and Instruction
FDA 3636
Laser Annual Report
Form and Instruction
FDA 3639
Cabinet X-Ray Product Report
Form and Instruction
FDA 3644
Therapy Ultrasound Product Report
Form and Instruction
FDA 3660
Microwave oven
Form and Instruction
FDA 3661
X-Ray Report
Form and Instruction
FDA 3662
Cephalometric Report
Form and Instruction
FDA 3663
Microwave products (non-oven)
(Burden Change Due to Rulemaking) Third party disclosure for Electronic Products: General Requirements
Modified
52
15508
0
Total burden requested under this ICR:
16763
404602
0
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