510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K946162Substantially Equivalent

3M(tm) Surgical Slipper, 9660 Series

Wahl Clipper Corp, Steriling IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K946162 is the FDA 510(k) clearance record for 3M(TM) SURGICAL SLIPPER, 9660 SERIES, a class I device, cleared for Wahl Clipper Corp. on under FDA product code LWK (Razor, Surgical). FDA records list 8 510(k) clearances for Wahl Clipper Corp., from to . As of , FDA records show no recalls naming K946162.

Clearance record

Decision date
Received
(36 days to decision)
Product code
LWK Razor, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Wahl Clipper Corp. 2900 N. Locust St., Steriling IL
510(k) summary
Summary
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