OXFORD RETRO-ILLUMINATION CATARACT CAMERA
K-Number: K873157 · 1987-09-30
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Device Summary
Frequently Asked Questions
What is the OXFORD RETRO-ILLUMINATION CATARACT CAMERA?
OXFORD RETRO-ILLUMINATION CATARACT CAMERA is a medical device that received FDA 510(k) clearance on 1987-09-30. The listed applicant is Holofax , Ltd.. The 510(k) number is K873157.
When did OXFORD RETRO-ILLUMINATION CATARACT CAMERA receive FDA 510(k) clearance?
OXFORD RETRO-ILLUMINATION CATARACT CAMERA received FDA 510(k) clearance on 1987-09-30, under 510(k) number K873157.
Who is the listed applicant for OXFORD RETRO-ILLUMINATION CATARACT CAMERA?
The FDA 510(k) record lists Holofax , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXFORD RETRO-ILLUMINATION CATARACT CAMERA?
The FDA product code for OXFORD RETRO-ILLUMINATION CATARACT CAMERA is HKI.
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: HKI)
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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