LRY — Punch, Surgical Class I

FDA Device Classification

FDA product code LRY covers "Punch, Surgical", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel. At least 7 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LRY
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K933516acudermACU-E PUNCHMarch 24, 1994
K904869kramer constELLIPSE PUNCHMarch 6, 1991
K902636lipogenLIPOGEN RHEUMELISA DSDNA ASSAYJune 28, 1990
K896303premier medicalBIOPSY PUNCHFebruary 13, 1990
K874356med-toolPIN PUNCHNovember 23, 1987
K874357med-toolTAPERED PUNCHNovember 23, 1987
K872388med-toolNAIL SETJuly 23, 1987