CLEARMEDICAL/HUNTLEIGH FOOT GARMENTS; MODELS FG200/LRG (LARGE), FG200/STD (STANDARD), FG100/SM (SMALL), FG100-R (REGULAR— 510(k) K012616

Name: FDA 510(k) clearance K012616
Creator: U.S. Food and Drug Administration
Published: 2002-02-06

Substantially Equivalent

Clearmedical, Inc.

FDA 510(k) clearance K012616 for CLEARMEDICAL/HUNTLEIGH FOOT GARMENTS; MODELS FG200/LRG (LARGE), FG200/STD (STANDARD), FG100/SM (SMALL), FG100-R (REGULAR, Substantially Equivalent on 2002-02-06. Applicant: Clearmedical, Inc.. Device class: 2.

Clearance details

Applicant: Clearmedical, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2001-08-13
Decision date: 2002-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellevue, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOW

view all

K261807 — Sequential Circulator (SC-4004-DL, SC-4008-DL)2026-09-11
K254217 — Aerloom2026-08-31
K253555 — Flexitouch® Plus Advanced Pneumatic Compression System2026-07-31
K253386 — DVT Garment2026-06-25
K250242 — Compression Therapy Device (LGT-2202DVT)2026-04-24

More clearances from Clearmedical, Inc.

view all

K033578 — REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS2005-07-11
K033579 — REPROCESSED MULTIPLE CLIP APPLIERS2005-07-11
K033591 — REPROCESSED TROCARS2005-06-03
K033592 — REPROCESSED SURGICAL SCISSORS AND GRASPERS2004-07-27
K033593 — REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS2003-11-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.