FDA 510(k)

RES-Q-MATE

K-Number: K841120 · 1984-04-05

Decision Date1984-04-05

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

RES-Q-MATE is the device name listed in this FDA 510(k) record. The listed applicant is Rsq Industries, Inc.. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K841120. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RES-Q-MATE?

RES-Q-MATE is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Rsq Industries, Inc.. The 510(k) number is K841120.

When did RES-Q-MATE receive FDA 510(k) clearance?

RES-Q-MATE received FDA 510(k) clearance on 1984-04-05, under 510(k) number K841120.

Who is the listed applicant for RES-Q-MATE?

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

What is the FDA product code for RES-Q-MATE?

The FDA product code for RES-Q-MATE is CAE.

Related Devices (Code: CAE)

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.

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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.