Product code FWD— General, Plastic Surgery

FDA has cleared 5 devices under product code FWD between 1986 and 1989, filed by 2 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.

• 19891 clearance
• 19881 clearance
• 19863 clearances

• Jedmed Instrument Co.4 clearances
• Medical Dynamics, Inc.1 clearance

• K891236 — FDX SOLID STATE VIDEO CAMERA MODEL 5950Medical Dynamics, Inc.·1989-04-05
• K882166 — JEDMED MICRO CCD CAMERA SYSTEMJedmed Instrument Co.·1988-06-15
• K862664 — JEDMED CCD CAMERA SYSTEMJedmed Instrument Co.·1986-07-30
• K862145 — JEDMED MINI-MOS VIDEO CAMERAJedmed Instrument Co.·1986-06-13
• K862034 — JEDMED CCD-02 VIDEO CAMERA SYSTEMJedmed Instrument Co.·1986-06-09