FDA 510(k)

TOA

K-Number: K972061 · 1997-08-21

Decision Date1997-08-21

Product CodeLRK

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

TOA is the device name listed in this FDA 510(k) record. The listed applicant is W. Keith Thornton, D.D.S.. It received FDA 510(k) clearance on 1997-08-21 under 510(k) number K972061. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOA?

TOA is a medical device that received FDA 510(k) clearance on 1997-08-21. The listed applicant is W. Keith Thornton, D.D.S.. The 510(k) number is K972061.

When did TOA receive FDA 510(k) clearance?

TOA received FDA 510(k) clearance on 1997-08-21, under 510(k) number K972061.

Who is the listed applicant for TOA?

The FDA 510(k) record lists W. Keith Thornton, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOA?

The FDA product code for TOA is LRK.

Other records listing W. Keith Thornton, D.D.S. 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.

K981744COMBINATION TOA WITH NASAL MASK HOLDER AND UNIVERSAL NASAL MASK HOLDER

Related Devices (Code: LRK)

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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.