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LWK — Razor, Surgical Class I

FDA Device Classification

Classification Details

Product Code
LWK
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
K946162wahl clipper3M(TM) SURGICAL SLIPPER, 9660 SERIESJanuary 24, 1995
K910524baxter healthcareSURGICAL CLIPPERMarch 28, 1991
K874370derma-safeSURGICAL PREP RAZORNovember 13, 1987
K874234derma-safeSURGICAL PREP RAZOR, STRAIGHT TYPENovember 2, 1987