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FDA 510(k)

MENTOR ANTERIOR SEGMENT VITRECTOR

K-Number: K890595 · 1989-04-17

ApplicantMentor O & O, Inc.
Decision Date1989-04-17
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENTOR ANTERIOR SEGMENT VITRECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Mentor O & O, Inc.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K890595. The device is classified under product code HKP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR ANTERIOR SEGMENT VITRECTOR?

MENTOR ANTERIOR SEGMENT VITRECTOR is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K890595.

When did MENTOR ANTERIOR SEGMENT VITRECTOR receive FDA 510(k) clearance?

MENTOR ANTERIOR SEGMENT VITRECTOR received FDA 510(k) clearance on 1989-04-17, under 510(k) number K890595.

Who is the listed applicant for MENTOR ANTERIOR SEGMENT VITRECTOR?

The FDA 510(k) record lists Mentor O & O, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENTOR ANTERIOR SEGMENT VITRECTOR?

The FDA product code for MENTOR ANTERIOR SEGMENT VITRECTOR is HKP.

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Other records listing Mentor O & O, 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.

K955245MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEMK934320MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATIONK912904MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEMK915340MENTOR HORIZON LOW VISION MAGNIFIERK910637MENTOR(R) SUR-E-TROL(R)K911160MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305

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Related Devices (Code: HKP)

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.

K952558AARON VAC 2Aaron Medical IndustriesK950056THE GRIESHABER AXIAL CUTTERGrieshaber & Co.K950287UNIVIT PROBEMedical Instrument Development Laboratories, Inc.K896622VISITEC VITRECTOMY UNITVisitec Co.K832074CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRACooperVision, Inc.K822599KEATES I/A SYSTEM FRIGITRONICS 4000Frigitronics of Connecticut, 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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