Product code KGY— General, Plastic Surgery

FDA has cleared 6 devices under product code KGY between 1980 and 1993, 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.

• 19931 clearance
• 19912 clearances
• 19831 clearance
• 19802 clearances

• Johnson & Johnson Professionals, Inc.2 clearances
• Megadyne Medical Products, Inc.1 clearance
• Medovations, Inc.1 clearance
• Cook Urological, Inc.1 clearance
• 3M Company1 clearance

• K933085 — GOODMAN BANDAGEMegadyne Medical Products, Inc.·1993-12-23
• K913678 — TROCAR CATHETERMedovations, Inc.·1991-12-16
• K910914 — SURGICAL TISSUE POUCHCook Urological, Inc.·1991-03-28
• K832318 — ISOLATION BAG 3M3M Company·1983-10-31
• K801823 — BAND-AID BRAND TRICOT MESH BANDAGESJohnson & Johnson Professionals, Inc.·1980-08-20
• K801824 — BAND-AID BRAND FLEXIBLE FABRIC BANDAGEJohnson & Johnson Professionals, Inc.·1980-08-20