ELASTIC COMPRESSION ANKLET
K-Number: K823350 · 1982-12-03
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Device Summary
Frequently Asked Questions
What is the ELASTIC COMPRESSION ANKLET?
ELASTIC COMPRESSION ANKLET is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Podiatry Products Corp.. The 510(k) number is K823350.
When did ELASTIC COMPRESSION ANKLET receive FDA 510(k) clearance?
ELASTIC COMPRESSION ANKLET received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823350.
Who is the listed applicant for ELASTIC COMPRESSION ANKLET?
The FDA 510(k) record lists Podiatry Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELASTIC COMPRESSION ANKLET?
The FDA product code for ELASTIC COMPRESSION ANKLET is FQL.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FQL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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