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FDA 510(k)

LANDERS VITRECTOMY LENS RING SYSTEMS

K-Number: K850991 · 1985-03-29

ApplicantOcular Instruments, Inc.
Decision Date1985-03-29
Product CodeHNH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LANDERS VITRECTOMY LENS RING SYSTEMS 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 1985-03-29 under 510(k) number K850991. 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 SYSTEMS?

LANDERS VITRECTOMY LENS RING SYSTEMS is a medical device that received FDA 510(k) clearance on 1985-03-29. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K850991.

When did LANDERS VITRECTOMY LENS RING SYSTEMS receive FDA 510(k) clearance?

LANDERS VITRECTOMY LENS RING SYSTEMS received FDA 510(k) clearance on 1985-03-29, under 510(k) number K850991.

Who is the listed applicant for LANDERS VITRECTOMY LENS RING SYSTEMS?

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 SYSTEMS?

The FDA product code for LANDERS VITRECTOMY LENS RING SYSTEMS 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.K902496LANDERS VITRECTOMY LENS RING W/INFUSIONOcular Instruments, Inc.K863775RK VACUUM FIXATION RING SYSTEMAmeritek, 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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