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FDA 510(k)

EMERGENCY FAST-FIX DENTURE REPAIR KIT

K-Number: K770091 · 1977-01-24

Decision Date1977-01-24
Product CodeEBO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EMERGENCY FAST-FIX DENTURE REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mr. Clarence Hurst. It received FDA 510(k) clearance on 1977-01-24 under 510(k) number K770091. The device is classified under product code EBO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERGENCY FAST-FIX DENTURE REPAIR KIT?

EMERGENCY FAST-FIX DENTURE REPAIR KIT is a medical device that received FDA 510(k) clearance on 1977-01-24. The listed applicant is Mr. Clarence Hurst. The 510(k) number is K770091.

When did EMERGENCY FAST-FIX DENTURE REPAIR KIT receive FDA 510(k) clearance?

EMERGENCY FAST-FIX DENTURE REPAIR KIT received FDA 510(k) clearance on 1977-01-24, under 510(k) number K770091.

Who is the listed applicant for EMERGENCY FAST-FIX DENTURE REPAIR KIT?

The FDA 510(k) record lists Mr. Clarence Hurst as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY FAST-FIX DENTURE REPAIR KIT?

The FDA product code for EMERGENCY FAST-FIX DENTURE REPAIR KIT is EBO.

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: EBO)

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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