510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K874234Substantially Equivalent

Surgical Prep Razor, Straight Type

Derma-Safe Co., Wayne NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874234 is the FDA 510(k) clearance record for SURGICAL PREP RAZOR, STRAIGHT TYPE, a class I device, cleared for Derma-Safe Co. on under FDA product code LWK (Razor, Surgical). FDA records list 2 510(k) clearances for Derma-Safe Co., from to . As of , FDA records show no recalls naming K874234.

Clearance record

Decision date
Received
(18 days to decision)
Product code
LWK Razor, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Derma-Safe Co. 32 Juniper Rd., Wayne NJ
Third party review
No

Clearances, product code LWK

Trailing 12 months

FDA records hold no clearances under product code LWK in the trailing twelve months.

FDA records show no clearances under product code LWK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LWK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260