Product code FZF— General, Plastic Surgery

FDA has cleared 7 devices under product code FZF between 1983 and 1988, filed by 4 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.

• 19881 clearance
• 19874 clearances
• 19851 clearance
• 19831 clearance

• Vinyl Technology, Inc.4 clearances
• Svenol Andersen1 clearance
• R. Evans Corp.1 clearance
• Hospitak, Inc.1 clearance

• K881516 — COMPRESAIDR. Evans Corp.·1988-04-29
• K874050 — INFLATABLE FOOT & ANKLE SPLINTVinyl Technology, Inc.·1987-11-23
• K874051 — INFLATABLE FULL LEG SPLINTVinyl Technology, Inc.·1987-11-23
• K874052 — INFLATABLE HALF LEG SPLINTVinyl Technology, Inc.·1987-11-23
• K874053 — INFLATABLE FULL ARM SPLINTVinyl Technology, Inc.·1987-11-23
• K853600 — INFLATABLE AIR SPLINTSHospitak, Inc.·1985-09-19
• K831764 — URIAS PRESSURE SPLINTS, & FIRST AIDSvenol Andersen·1983-09-12