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FDA 510(k)

COOLING TEETHERS

K-Number: K902974 · 1991-04-03

Decision Date1991-04-03
Product CodeKKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COOLING TEETHERS is the device name listed in this FDA 510(k) record. The listed applicant is Realgrow Intl. Corp.. It received FDA 510(k) clearance on 1991-04-03 under 510(k) number K902974. The device is classified under product code KKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOLING TEETHERS?

COOLING TEETHERS is a medical device that received FDA 510(k) clearance on 1991-04-03. The listed applicant is Realgrow Intl. Corp.. The 510(k) number is K902974.

When did COOLING TEETHERS receive FDA 510(k) clearance?

COOLING TEETHERS received FDA 510(k) clearance on 1991-04-03, under 510(k) number K902974.

Who is the listed applicant for COOLING TEETHERS?

The FDA 510(k) record lists Realgrow Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOLING TEETHERS?

The FDA product code for COOLING TEETHERS is KKO.

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: KKO)

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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