Product code FZQ— General, Plastic Surgery

FDA has cleared 6 devices under product code FZQ between 1982 and 1988, filed by 6 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
• 19871 clearance
• 19832 clearances
• 19822 clearances

• Temp-Stik Corp.1 clearance
• Surgeons Choice, Inc.1 clearance
• Richard-Allan Medical Ind., Inc.1 clearance
• Beiersdorf, Inc.1 clearance
• Alto Development Corp.1 clearance
• Acme United Corp.1 clearance

• K884783 — RANEY CLIPAlto Development Corp.·1988-11-30
• K873744 — LEUKOCLIP(R)Beiersdorf, Inc.·1987-09-30
• K830704 — ONE TIME DISPOSABLE SKIN STAPLERAcme United Corp.·1983-04-12
• K830768 — DISPOSABLE SKIN STAPLERSurgeons Choice, Inc.·1983-04-12
• K822963 — SURGICAL PRODUCTS, SKIN STAPLE REMOVERTemp-Stik Corp.·1982-11-08
• K822145 — COMPLETERichard-Allan Medical Ind., Inc.·1982-10-22