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FDA 510(k)

WINCO STRETCHAIR

K-Number: K110671 · 2011-04-22

Decision Date2011-04-22
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WINCO STRETCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Winco Mfg., LLC. It received FDA 510(k) clearance on 2011-04-22 under 510(k) number K110671. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINCO STRETCHAIR?

WINCO STRETCHAIR is a medical device that received FDA 510(k) clearance on 2011-04-22. The listed applicant is Winco Mfg., LLC. The 510(k) number is K110671.

When did WINCO STRETCHAIR receive FDA 510(k) clearance?

WINCO STRETCHAIR received FDA 510(k) clearance on 2011-04-22, under 510(k) number K110671.

Who is the listed applicant for WINCO STRETCHAIR?

The FDA 510(k) record lists Winco Mfg., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WINCO STRETCHAIR?

The FDA product code for WINCO STRETCHAIR is INK.

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: INK)

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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