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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