Product code GAO— General, Plastic Surgery

FDA has cleared 4 devices under product code GAO between 1980 and 1994, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19941 clearance
• 19871 clearance
• 19861 clearance
• 19801 clearance

• Unoplast A/S1 clearance
• United States Surgical, A Division of Tyco Healthc1 clearance
• Chathamborough Research Group, Inc.1 clearance
• Alto Development Corp.1 clearance

• K932513 — LABELING FOR MYO/WIRE II STERNOTOMY SUTURESAlto Development Corp.·1994-01-07
• K872532 — AUTO SUTURE STAINLESS STEEL SUTURES*United States Surgical, A Division of Tyco Healthc·1987-08-05
• K863034 — SHARPOINT STAINLESS STEEL SUTUREChathamborough Research Group, Inc.·1986-09-30
• K802248 — DISARP ORIGINALUnoplast A/S·1980-09-26