Product code FSD— General Hospital

FDA has cleared 5 devices under product code FSD between 1976 and 1989, 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.

• 19891 clearance
• 19831 clearance
• 19811 clearance
• 19771 clearance
• 19761 clearance

• Tecnol New Jersey Wound Care, Inc.1 clearance
• R.G. Moore1 clearance
• Oticon Corp.1 clearance
• Kuhn Industries1 clearance
• Fidelty Hearing Instruments, Inc.1 clearance

• K892379 — THE POUCH GROIN & ABDOMINAL STRESS AIDKuhn Industries·1989-07-20
• K822817 — DOCE ALL-IN-THE-EAR AIDFidelty Hearing Instruments, Inc.·1983-01-18
• K810379 — EARETTE HEARING AID SEARS #8054Oticon Corp.·1981-03-04
• K770162 — MATERNITY SUPPORTERR.G. Moore·1977-02-09
• K760772 — DISPOSABLE ABDOMINAL BINDERTecnol New Jersey Wound Care, Inc.·1976-11-03