Product code LRY— General, Plastic Surgery

FDA has cleared 7 devices under product code LRY between 1987 and 1994, filed by 5 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.

• 19941 clearance
• 19911 clearance
• 19902 clearances
• 19873 clearances

• Med-Tool, Inc.3 clearances
• Premier Medical1 clearance
• Lipogen, Inc.1 clearance
• Kramer Const1 clearance
• Acuderm, Inc.1 clearance

• K933516 — ACU-E PUNCHAcuderm, Inc.·1994-03-24
• K904869 — ELLIPSE PUNCHKramer Const·1991-03-06
• K902636 — LIPOGEN RHEUMELISA DSDNA ASSAYLipogen, Inc.·1990-06-28
• K896303 — BIOPSY PUNCHPremier Medical·1990-02-13
• K874356 — PIN PUNCHMed-Tool, Inc.·1987-11-23
• K874357 — TAPERED PUNCHMed-Tool, Inc.·1987-11-23
• K872388 — NAIL SETMed-Tool, Inc.·1987-07-23