KEELER/KONAN SPECULAR MICROSCOPE
K-Number: K810403 · 1981-05-13
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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