Product code FWB— General, Plastic Surgery

FDA has cleared 6 devices under product code FWB between 1982 and 1994, filed by 5 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19941 clearance
• 19901 clearance
• 19881 clearance
• 19871 clearance
• 19861 clearance
• 19821 clearance

• M.P. Video, Inc.2 clearances
• Sony Corp. of America1 clearance
• Seitz Technical Products, Inc.1 clearance
• Medline Industries, Inc.1 clearance
• Envision Medical Corp.1 clearance

• K934092 — CAMERA, SURGICAL AND ACCESSORIESEnvision Medical Corp.·1994-01-07
• K902359 — SURGICAL VIDEO CAMERA, MODEL 9500Seitz Technical Products, Inc.·1990-07-12
• K884343 — SONY COLOR VIDEO CAMERAS AND ACCESSORIESSony Corp. of America·1988-11-01
• K871057 — MC-SERIES SURGICAL CAMERASM.P. Video, Inc.·1987-04-03
• K855020 — MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930Medline Industries, Inc.·1986-01-24
• K820829 — MEDICAMM.P. Video, Inc.·1982-05-03