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FDA 510(k)

MENTOR POTENTIAL ACUITY METER

K-Number: K821932 · 1982-08-03

ApplicantMentor O & O, Inc.
Decision Date1982-08-03
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENTOR POTENTIAL ACUITY METER 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 1982-08-03 under 510(k) number K821932. 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 POTENTIAL ACUITY METER?

MENTOR POTENTIAL ACUITY METER is a medical device that received FDA 510(k) clearance on 1982-08-03. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K821932.

When did MENTOR POTENTIAL ACUITY METER receive FDA 510(k) clearance?

MENTOR POTENTIAL ACUITY METER received FDA 510(k) clearance on 1982-08-03, under 510(k) number K821932.

Who is the listed applicant for MENTOR POTENTIAL ACUITY METER?

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 POTENTIAL ACUITY METER?

The FDA product code for MENTOR POTENTIAL ACUITY METER 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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