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FDA 510(k)

SUPERSTAND STAND-UP WHELLCHAIR

K-Number: K962278 · 1996-10-02

Decision Date1996-10-02
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPERSTAND STAND-UP WHELLCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is The Standing Co., Inc.. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K962278. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERSTAND STAND-UP WHELLCHAIR?

SUPERSTAND STAND-UP WHELLCHAIR is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is The Standing Co., Inc.. The 510(k) number is K962278.

When did SUPERSTAND STAND-UP WHELLCHAIR receive FDA 510(k) clearance?

SUPERSTAND STAND-UP WHELLCHAIR received FDA 510(k) clearance on 1996-10-02, under 510(k) number K962278.

Who is the listed applicant for SUPERSTAND STAND-UP WHELLCHAIR?

The FDA 510(k) record lists The Standing Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERSTAND STAND-UP WHELLCHAIR?

The FDA product code for SUPERSTAND STAND-UP WHELLCHAIR is IPL.

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 The Standing Co., Inc. 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.

Related Devices (Code: IPL)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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