Product code GCC— General, Plastic Surgery

FDA has cleared 5 devices under product code GCC between 1982 and 1998, filed by 3 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.

• 19981 clearance
• 19921 clearance
• 19901 clearance
• 19891 clearance
• 19821 clearance

• Medical Engineering and Development Institute2 clearances
• Med Institute, Inc.2 clearances
• Van-Tec, Inc.1 clearance

Death

3

Total

3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

• K981061 — INTRAVASCULAR RETRIEVAL DEVICEMed Institute, Inc.·1998-05-26
• K922354 — BYRD TELESCOPING STAINLESS STEEL DILAT SHEATH SETMed Institute, Inc.·1992-07-30
• K902502 — BYRD STAINLESS STEEL DILATORMedical Engineering and Development Institute·1990-08-07
• K893480 — BYRD EXTRACTOR SETMedical Engineering and Development Institute·1989-06-23
• K820865 — VAN-TEC FASCIAL DILATORVan-Tec, Inc.·1982-05-05