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FDA 510(k)

PEDIATRIC VITRECTOMY LENS SET

K-Number: K914051 · 1991-12-09

Decision Date1991-12-09
Product CodeHJK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC VITRECTOMY LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Instruments, Inc.. It received FDA 510(k) clearance on 1991-12-09 under 510(k) number K914051. The device is classified under product code HJK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC VITRECTOMY LENS SET?

PEDIATRIC VITRECTOMY LENS SET is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K914051.

When did PEDIATRIC VITRECTOMY LENS SET receive FDA 510(k) clearance?

PEDIATRIC VITRECTOMY LENS SET received FDA 510(k) clearance on 1991-12-09, under 510(k) number K914051.

Who is the listed applicant for PEDIATRIC VITRECTOMY LENS SET?

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 PEDIATRIC VITRECTOMY LENS SET?

The FDA product code for PEDIATRIC VITRECTOMY LENS SET 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.

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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

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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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