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FDA 510(k)

VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE

K-Number: K882634 · 1988-07-15

ApplicantVistech Consultants, Inc.
Decision Date1988-07-15
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE is the device name listed in this FDA 510(k) record. The listed applicant is Vistech Consultants, Inc.. It received FDA 510(k) clearance on 1988-07-15 under 510(k) number K882634. 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 VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE?

VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE is a medical device that received FDA 510(k) clearance on 1988-07-15. The listed applicant is Vistech Consultants, Inc.. The 510(k) number is K882634.

When did VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE receive FDA 510(k) clearance?

VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE received FDA 510(k) clearance on 1988-07-15, under 510(k) number K882634.

Who is the listed applicant for VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE?

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

What is the FDA product code for VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE?

The FDA product code for VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE is HOX.

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Other records listing Vistech Consultants, 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.

K881059MCT 8000 (MULTI-VISION CONTRAST TESTER)K881021VCTS 700S SYSTEMK881022VCTS MARKETING PROGRAM SYSTEMK881023VCTS 6500 SYSTEMK853481VISTECH VCTS GLARE TESTERK840255VISTECH VCTS 6000

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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.K881358PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAMNeuroscientific Corp.K881059MCT 8000 (MULTI-VISION CONTRAST TESTER)Vistech Consultants, 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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