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FDA 510(k)

LANDERS VITRECTOMY LENS RING W/INFUSION

K-Number: K902496 · 1990-07-24

ApplicantOcular Instruments, Inc.
Decision Date1990-07-24
Product CodeHNH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LANDERS VITRECTOMY LENS RING W/INFUSION 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 1990-07-24 under 510(k) number K902496. The device is classified under product code HNH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANDERS VITRECTOMY LENS RING W/INFUSION?

LANDERS VITRECTOMY LENS RING W/INFUSION is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K902496.

When did LANDERS VITRECTOMY LENS RING W/INFUSION receive FDA 510(k) clearance?

LANDERS VITRECTOMY LENS RING W/INFUSION received FDA 510(k) clearance on 1990-07-24, under 510(k) number K902496.

Who is the listed applicant for LANDERS VITRECTOMY LENS RING W/INFUSION?

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 LANDERS VITRECTOMY LENS RING W/INFUSION?

The FDA product code for LANDERS VITRECTOMY LENS RING W/INFUSION is HNH.

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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.

K014170STAURENGHI WIDE FIELD SCANNING LASER LENSK012096DISPOSABLE VITRECTOMY LENSK933976MANDELKORN SUTURE LYSIS LENSK933264RITCH NYLON SUTURE LASER LENSK94142050 DEGREE HRI PRISM LENSK935302OSHER SURGICAL GONIO/POSTERIOR POLE LENS

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Related Devices (Code: HNH)

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.

K912269LANDERS NOTCHED IRRIGATING VITRECTOMY LENS RINGOcular Instruments, Inc.K912268LANDERS NOTCHED VITRECTOMY LENS RINGOcular Instruments, Inc.K912151LANDERS THREE STRUT VITRECTOMY LENS RINGOcular Instruments, Inc.K863775RK VACUUM FIXATION RING SYSTEMAmeritek, Inc.K850991LANDERS VITRECTOMY LENS RING SYSTEMSOcular Instruments, Inc.K832912GELENDER VACUUM FIXATION RING SYSMiami Eye Technology, Inc.

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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