DISPOSABLE VITRECTOMY LENS
K-Number: K012096 · 2001-08-24
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE VITRECTOMY LENS?
DISPOSABLE VITRECTOMY LENS is a medical device that received FDA 510(k) clearance on 2001-08-24. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K012096.
When did DISPOSABLE VITRECTOMY LENS receive FDA 510(k) clearance?
DISPOSABLE VITRECTOMY LENS received FDA 510(k) clearance on 2001-08-24, under 510(k) number K012096.
Who is the listed applicant for DISPOSABLE 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 DISPOSABLE VITRECTOMY LENS?
The FDA product code for DISPOSABLE 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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