Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K012616Substantially Equivalent

Clearmedical/huntleigh Foot Garments; Models Fg200/lrg (Large), Fg200/std (Standard), Fg100/sm (Small), Fg100-R (Regular

Clearmedical, Inc., Bellevue WA / Traditional, Substantially Equivalent

K012616 is the FDA 510(k) clearance record for CLEARMEDICAL/HUNTLEIGH FOOT GARMENTS; MODELS FG200/LRG (LARGE), FG200/STD (STANDARD), FG100/SM (SMALL), FG100-R (REGULAR, a class II device, cleared for Clearmedical, Inc. on under FDA product code JOW (Sleeve, Limb, Compressible). FDA records list 14 510(k) clearances for Clearmedical, Inc., from to . As of , FDA records show no recalls naming K012616.

Clearance record

Decision date
Received
(177 days to decision)
Product code
JOW Sleeve, Limb, Compressible
Regulation
21 CFR 870.5800
Device class
Class II
Review panel
Cardiovascular
Applicant
Clearmedical, Inc. 1776 136th Pl. NE, Bellevue WA
510(k) summary
Summary
Third party review
No

Clearances, product code JOW

Trailing 12 months
8 clearances under product code JOW in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JOW, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20261
March 20260
April 20261
May 20260
June 20261
July 20261
August 20261
September 20261
October 20260