Product code DWG— General, Plastic Surgery

FDA has cleared 4 devices under product code DWG between 1993 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.

• 19943 clearances
• 19931 clearance

• Mahe Intl., Inc.1 clearance
• Conmedcorp1 clearance
• Beacon Laboratories, Inc.1 clearance
• Aspen Labs1 clearance

• K942823 — MAHE INSTRUMENTSMahe Intl., Inc.·1994-12-05
• K932345 — TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USEConmedcorp·1994-04-12
• K931215 — HAND-TROL SAspen Labs·1994-03-28
• K925708 — DISPOSABLE ELECTROSURGERY BALL ELECTRODEBeacon Laboratories, Inc.·1993-04-20