Product Code: FWL FDA class 1 21 CFR 878.4160

Camera, Cine, Endoscopic, Without Audio

General, Plastic Surgery

An endoscopic cine camera without audio is a motion picture recording device used in conjunction with endoscopic equipment to capture video footage of internal structures during minimally invasive procedures, without sound. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FWL, regulated under 21 CFR 878.4160, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k)s
2
FEI Numbers
35
Registration Numbers
35
Unique Applicants
2
Years Active
7

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Basic Information

Product Code
FWL
Device Class
FDA class 1
Regulation Number
878.4160
Medical Specialty
General, Plastic Surgery
Review Panel
SU
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 2 510(k) clearances via K numbers.

K Number Device Name
K951519 WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT
K883760 STORZ MODEL 62 ENT CAMERA SYSTEM

FEI Numbers

This FDA classification entry is associated with 35 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 35 registration numbers. Click on an entry to view related FDA registrations.