510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K241746Substantially Equivalent

Umed Reprocessed Aircast Venaflow Foot Cuff; Umed Reprocessed Kendall Scd Express Sleeve; Umed Reprocessed Aircast Elite Calf Cuff 3040 3050; Umed Reprocessed Ctc Vp 501 Calf Cuff; Umed Reprocessed Ctc Vp 520 Foot Cuff

United Medical Resources LLC, North Salt Lake UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K241746 is the FDA 510(k) clearance record for UMED REPROCESSED AIRCAST VENAFLOW FOOT CUFF; UMED REPROCESSED KENDALL SCD EXPRESS SLEEVE; UMED REPROCESSED AIRCAST ELITE CALF CUFF 3040 3050; UMED REPROCESSED CTC VP 501 CALF CUFF; UMED REPROCESSED CTC VP 520 FOOT CUFF, a class II device, cleared for United Medical Resources, LLC on under FDA product code JOW (Sleeve, Limb, Compressible). FDA records list one 510(k) clearance for United Medical Resources, LLC. As of , FDA records show no recalls naming K241746.

Clearance record

Decision date
Received
(108 days to decision)
Product code
JOW Sleeve, Limb, Compressible
Regulation
21 CFR 870.5800
Device class
Class II
Review panel
Cardiovascular
Applicant
United Medical Resources, LLC 270 W 500 N, North Salt Lake UT
510(k) summary
Statement
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