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FDA 510(k)

KEELER/KONAN SPECULAR MICROSCOPE

K-Number: K810403 · 1981-05-13

Decision Date1981-05-13
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KEELER/KONAN SPECULAR MICROSCOPE 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 1981-05-13 under 510(k) number K810403. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEELER/KONAN SPECULAR MICROSCOPE?

KEELER/KONAN SPECULAR MICROSCOPE is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Keeler Optical Products , Ltd.. The 510(k) number is K810403.

When did KEELER/KONAN SPECULAR MICROSCOPE receive FDA 510(k) clearance?

KEELER/KONAN SPECULAR MICROSCOPE received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810403.

Who is the listed applicant for KEELER/KONAN SPECULAR MICROSCOPE?

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 KEELER/KONAN SPECULAR MICROSCOPE?

The FDA product code for KEELER/KONAN SPECULAR MICROSCOPE is HJO.

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: HJO)

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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