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FDA 510(k)

MENTOR BRIGHTNESS ACUITY TESTER

K-Number: K853736 · 1985-11-01

ApplicantMentor O & O, Inc.
Decision Date1985-11-01
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENTOR BRIGHTNESS ACUITY 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 1985-11-01 under 510(k) number K853736. 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 BRIGHTNESS ACUITY TESTER?

MENTOR BRIGHTNESS ACUITY TESTER is a medical device that received FDA 510(k) clearance on 1985-11-01. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K853736.

When did MENTOR BRIGHTNESS ACUITY TESTER receive FDA 510(k) clearance?

MENTOR BRIGHTNESS ACUITY TESTER received FDA 510(k) clearance on 1985-11-01, under 510(k) number K853736.

Who is the listed applicant for MENTOR BRIGHTNESS ACUITY 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 BRIGHTNESS ACUITY TESTER?

The FDA product code for MENTOR BRIGHTNESS ACUITY 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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