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FDA 510(k)

HUTT SWIVEL WALKER & HUTT STANDING FRAME

K-Number: K812903 · 1982-02-05

Decision Date1982-02-05
Product Code
DecisionSubstantially Equivalent

Device Summary

HUTT SWIVEL WALKER & HUTT STANDING FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Barnett Medical. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K812903. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUTT SWIVEL WALKER & HUTT STANDING FRAME?

HUTT SWIVEL WALKER & HUTT STANDING FRAME is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Barnett Medical. The 510(k) number is K812903.

When did HUTT SWIVEL WALKER & HUTT STANDING FRAME receive FDA 510(k) clearance?

HUTT SWIVEL WALKER & HUTT STANDING FRAME received FDA 510(k) clearance on 1982-02-05, under 510(k) number K812903.

Who is the listed applicant for HUTT SWIVEL WALKER & HUTT STANDING FRAME?

The FDA 510(k) record lists Barnett Medical as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Barnett Medical as applicant

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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