Product code GBC— General, Plastic Surgery

FDA has cleared 4 devices under product code GBC between 1981 and 1990, 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.

• 19901 clearance
• 19831 clearance
• 19812 clearances

• Skytron, Div. the Kmw Group, Inc.1 clearance
• Sil-Med Corp.1 clearance
• Jedmed Instrument Co.1 clearance
• Cavitron Corp.1 clearance

• K896961 — HALUX EXLITE MINOR SURGERY LIGHTJedmed Instrument Co.·1990-02-22
• K830610 — FLAT SUCTION DRAINSil-Med Corp.·1983-03-29
• K811311 — SKYTRON ELITE SURGICAL TABLESSkytron, Div. the Kmw Group, Inc.·1981-06-02
• K810207 — MINOR SURGERY LIGHTCavitron Corp.·1981-02-13