Product code LWK— General, Plastic Surgery

FDA has cleared 4 devices under product code LWK between 1987 and 1995, filed by 3 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.

• 19951 clearance
• 19911 clearance
• 19872 clearances

• Derma-Safe Co.2 clearances
• Wahl Clipper Corp.1 clearance
• Baxter Healthcare Corp1 clearance

• K946162 — 3M(TM) SURGICAL SLIPPER, 9660 SERIESWahl Clipper Corp.·1995-01-24
• K910524 — SURGICAL CLIPPERBaxter Healthcare Corp·1991-03-28
• K874370 — SURGICAL PREP RAZORDerma-Safe Co.·1987-11-13
• K874234 — SURGICAL PREP RAZOR, STRAIGHT TYPEDerma-Safe Co.·1987-11-02