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FDA 510(k)

THE PROGRESSIVE CHAIR

K-Number: K823277 · 1982-12-13

Decision Date1982-12-13
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE PROGRESSIVE CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Productions , Ltd.. It received FDA 510(k) clearance on 1982-12-13 under 510(k) number K823277. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PROGRESSIVE CHAIR?

THE PROGRESSIVE CHAIR is a medical device that received FDA 510(k) clearance on 1982-12-13. The listed applicant is Progressive Productions , Ltd.. The 510(k) number is K823277.

When did THE PROGRESSIVE CHAIR receive FDA 510(k) clearance?

THE PROGRESSIVE CHAIR received FDA 510(k) clearance on 1982-12-13, under 510(k) number K823277.

Who is the listed applicant for THE PROGRESSIVE CHAIR?

The FDA 510(k) record lists Progressive Productions , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PROGRESSIVE CHAIR?

The FDA product code for THE PROGRESSIVE CHAIR is INN.

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 Progressive Productions , Ltd. 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: INN)

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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