Product code DWH— General, Plastic Surgery

FDA has cleared 4 devices under product code DWH between 1983 and 1990, filed by 4 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.

• 19901 clearance
• 19861 clearance
• 19851 clearance
• 19831 clearance

• Temp Medical Products, Inc.1 clearance
• Micro-Aire Surgical Instruments, Inc.1 clearance
• Hall Surgical, Division of Zimmer, Inc.1 clearance
• Codman & Shurtleff, Inc.1 clearance

• K904352 — CODMAN COLLINS RADIOPARENT STERNAL BLADESCodman & Shurtleff, Inc.·1990-11-21
• K862474 — HALL STERNUM SAWHall Surgical, Division of Zimmer, Inc.·1986-07-17
• K850483 — MICRO-AIRE STERNUM SAW REPLACEMENT BLADESMicro-Aire Surgical Instruments, Inc.·1985-03-01
• K830189 — CARDIOVASCULAR SAW BLADESTemp Medical Products, Inc.·1983-03-24