ELASTIC COMPRESSION ANKLET— 510(k) K823350

Name: FDA 510(k) clearance K823350
Creator: U.S. Food and Drug Administration
Published: 1982-12-03

Substantially Equivalent

Podiatry Products Corp.

FDA 510(k) clearance K823350 for ELASTIC COMPRESSION ANKLET, Substantially Equivalent on 1982-12-03. Applicant: Podiatry Products Corp.. Device class: 1.

Clearance details

Applicant: Podiatry Products Corp.
Product code: Code FQL
Device class: Class 1
Regulation: 21 CFR 880.5780
Advisory panel: General Hospital
Date received: 1982-11-09
Decision date: 1982-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FQL

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K944240 — SOFT SOCK1994-12-27
K823789 — ELASTIC COMPRESSION ANKLET1983-01-07
K821259 — VITASAN1982-06-23
K821260 — VITOFIT1982-06-23
K820484 — VENES CUSTON RX1982-03-18

Adverse events under product code FQL

product code FQL

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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