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FDA 510(k)

MEYER FOREIGN BODY LOCATOR

K-Number: K920470 · 1992-08-26

Decision Date1992-08-26
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEYER FOREIGN BODY LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Seymour W. Meyer. It received FDA 510(k) clearance on 1992-08-26 under 510(k) number K920470. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEYER FOREIGN BODY LOCATOR?

MEYER FOREIGN BODY LOCATOR is a medical device that received FDA 510(k) clearance on 1992-08-26. The listed applicant is Seymour W. Meyer. The 510(k) number is K920470.

When did MEYER FOREIGN BODY LOCATOR receive FDA 510(k) clearance?

MEYER FOREIGN BODY LOCATOR received FDA 510(k) clearance on 1992-08-26, under 510(k) number K920470.

Who is the listed applicant for MEYER FOREIGN BODY LOCATOR?

The FDA 510(k) record lists Seymour W. Meyer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEYER FOREIGN BODY LOCATOR?

The FDA product code for MEYER FOREIGN BODY LOCATOR is IZH.

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: IZH)

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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