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FDA 510(k)

ELASTIC COMPRESSION ANKLET

K-Number: K823789 · 1983-01-07

ApplicantOrthopaedic Resources Corp.
Decision Date1983-01-07
Product CodeFQL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELASTIC COMPRESSION ANKLET is the device name listed in this FDA 510(k) record. The listed applicant is Orthopaedic Resources Corp.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K823789. The device is classified under product code FQL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELASTIC COMPRESSION ANKLET?

ELASTIC COMPRESSION ANKLET is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Orthopaedic Resources Corp.. The 510(k) number is K823789.

When did ELASTIC COMPRESSION ANKLET receive FDA 510(k) clearance?

ELASTIC COMPRESSION ANKLET received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823789.

Who is the listed applicant for ELASTIC COMPRESSION ANKLET?

The FDA 510(k) record lists Orthopaedic Resources 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

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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.

K944240SOFT SOCKSilipos, Inc.K823350ELASTIC COMPRESSION ANKLETPodiatry Products Corp.K821260VITOFITSelomas, Inc.K821259VITASANSelomas, Inc.K820484VENES CUSTON RXJung Products, Inc.

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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