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FDA 510(k)

INVERCHAIR

K-Number: K821002 · 1982-06-22

ApplicantInverchair Marketing, Inc.
Decision Date1982-06-22
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INVERCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Inverchair Marketing, Inc.. It received FDA 510(k) clearance on 1982-06-22 under 510(k) number K821002. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVERCHAIR?

INVERCHAIR is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Inverchair Marketing, Inc.. The 510(k) number is K821002.

When did INVERCHAIR receive FDA 510(k) clearance?

INVERCHAIR received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821002.

Who is the listed applicant for INVERCHAIR?

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

What is the FDA product code for INVERCHAIR?

The FDA product code for INVERCHAIR is ITH.

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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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