510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823350Substantially Equivalent

Elastic Compression Anklet

Podiatry Products Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823350 is the FDA 510(k) clearance record for ELASTIC COMPRESSION ANKLET, a class I device, cleared for Podiatry Products Corp. on under FDA product code FQL (Stocking, Medical Support (For General Medical Purposes)). FDA records list one 510(k) clearance for Podiatry Products Corp. As of , FDA records show no recalls naming K823350.

Clearance record

Decision date
Received
(24 days to decision)
Product code
FQL Stocking, Medical Support (For General Medical Purposes)
Regulation
21 CFR 880.5780
Device class
Class I
Review panel
General Hospital
Applicant
Podiatry Products Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FQL

Trailing 12 months

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

FDA records show no clearances under product code FQL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FQL, 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