BICONCAVE VITRECTOMY LENS
K-Number: K875331 · 1988-02-26
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Device Summary
Frequently Asked Questions
What is the BICONCAVE VITRECTOMY LENS?
BICONCAVE VITRECTOMY LENS is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K875331.
When did BICONCAVE VITRECTOMY LENS receive FDA 510(k) clearance?
BICONCAVE VITRECTOMY LENS received FDA 510(k) clearance on 1988-02-26, under 510(k) number K875331.
Who is the listed applicant for BICONCAVE VITRECTOMY LENS?
The FDA 510(k) record lists Ocular Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BICONCAVE VITRECTOMY LENS?
The FDA product code for BICONCAVE VITRECTOMY LENS is HJK.
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 Ocular Instruments, Inc. 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: HJK)
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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