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FDA 510(k)

LOCATOR, FOREIGN BODY

K-Number: K781892 · 1978-12-04

Decision Date1978-12-04
Product CodeHPM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOCATOR, FOREIGN BODY is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Optical Products , Ltd.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781892. The device is classified under product code HPM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCATOR, FOREIGN BODY?

LOCATOR, FOREIGN BODY is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Keeler Optical Products , Ltd.. The 510(k) number is K781892.

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

LOCATOR, FOREIGN BODY received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781892.

Who is the listed applicant for LOCATOR, FOREIGN BODY?

The FDA 510(k) record lists Keeler Optical Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for LOCATOR, FOREIGN BODY is HPM.

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 Keeler Optical Products , Ltd. 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: HPM)

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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