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FDA 510(k)

MENTOR B-VAT(TM) II VIDEO TESTER

K-Number: K875112 · 1988-03-08

ApplicantMentor O & O, Inc.
Decision Date1988-03-08
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENTOR B-VAT(TM) II VIDEO TESTER 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 1988-03-08 under 510(k) number K875112. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR B-VAT(TM) II VIDEO TESTER?

MENTOR B-VAT(TM) II VIDEO TESTER is a medical device that received FDA 510(k) clearance on 1988-03-08. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K875112.

When did MENTOR B-VAT(TM) II VIDEO TESTER receive FDA 510(k) clearance?

MENTOR B-VAT(TM) II VIDEO TESTER received FDA 510(k) clearance on 1988-03-08, under 510(k) number K875112.

Who is the listed applicant for MENTOR B-VAT(TM) II VIDEO TESTER?

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 B-VAT(TM) II VIDEO TESTER?

The FDA product code for MENTOR B-VAT(TM) II VIDEO TESTER is HOX.

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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: HOX)

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.

K100095CENTRAL VISION ANALYZER MODEL 1000Vimetrics,Llc.K944156HEINE LAMBDA 100Heine USA , Ltd.K881971OCCU-TECH VISION TESTApplied Vision Concepts, Inc.K883337PL 20/20 INFANT VISION TESTEROptimed Technologies, Inc.K882634VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLAREVistech Consultants, Inc.K881358PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAMNeuroscientific Corp.

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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