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FDA 510(k)

INGROWN TOENAIL APPLIANCE, OR

K-Number: K781135 · 1978-08-14

Decision Date1978-08-14
Product Code
DecisionSubstantially Equivalent

Device Summary

INGROWN TOENAIL APPLIANCE, OR is the device name listed in this FDA 510(k) record. The listed applicant is Barmore, Barbara. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781135. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INGROWN TOENAIL APPLIANCE, OR?

INGROWN TOENAIL APPLIANCE, OR is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Barmore, Barbara. The 510(k) number is K781135.

When did INGROWN TOENAIL APPLIANCE, OR receive FDA 510(k) clearance?

INGROWN TOENAIL APPLIANCE, OR received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781135.

Who is the listed applicant for INGROWN TOENAIL APPLIANCE, OR?

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

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.

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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