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FDA 510(k)

FOLDING ROLL-ABOUT CHAIR

K-Number: K802744 · 1980-11-19

Decision Date1980-11-19
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FOLDING ROLL-ABOUT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Winco Winfield Co., Inc.. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802744. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOLDING ROLL-ABOUT CHAIR?

FOLDING ROLL-ABOUT CHAIR is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Winco Winfield Co., Inc.. The 510(k) number is K802744.

When did FOLDING ROLL-ABOUT CHAIR receive FDA 510(k) clearance?

FOLDING ROLL-ABOUT CHAIR received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802744.

Who is the listed applicant for FOLDING ROLL-ABOUT CHAIR?

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

What is the FDA product code for FOLDING ROLL-ABOUT CHAIR?

The FDA product code for FOLDING ROLL-ABOUT CHAIR is INM.

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 Winco Winfield 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: INM)

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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