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FDA 510(k)

GOLDSMITH & REVERE TENARY ALLOY

K-Number: K821222 · 1982-05-24

Decision Date1982-05-24
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GOLDSMITH & REVERE TENARY ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Goldsmith & Revere, Inc.. It received FDA 510(k) clearance on 1982-05-24 under 510(k) number K821222. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLDSMITH & REVERE TENARY ALLOY?

GOLDSMITH & REVERE TENARY ALLOY is a medical device that received FDA 510(k) clearance on 1982-05-24. The listed applicant is Goldsmith & Revere, Inc.. The 510(k) number is K821222.

When did GOLDSMITH & REVERE TENARY ALLOY receive FDA 510(k) clearance?

GOLDSMITH & REVERE TENARY ALLOY received FDA 510(k) clearance on 1982-05-24, under 510(k) number K821222.

Who is the listed applicant for GOLDSMITH & REVERE TENARY ALLOY?

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

What is the FDA product code for GOLDSMITH & REVERE TENARY ALLOY?

The FDA product code for GOLDSMITH & REVERE TENARY ALLOY is EJJ.

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.

Other records listing Goldsmith & Revere, Inc. 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.

Related Devices (Code: EJJ)

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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