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FDA 510(k)

PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM

K-Number: K881358 · 1988-06-27

ApplicantNeuroscientific Corp.
Decision Date1988-06-27
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Neuroscientific Corp.. It received FDA 510(k) clearance on 1988-06-27 under 510(k) number K881358. 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 PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM?

PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM is a medical device that received FDA 510(k) clearance on 1988-06-27. The listed applicant is Neuroscientific Corp.. The 510(k) number is K881358.

When did PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM receive FDA 510(k) clearance?

PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM received FDA 510(k) clearance on 1988-06-27, under 510(k) number K881358.

Who is the listed applicant for PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM?

The FDA 510(k) record lists Neuroscientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM?

The FDA product code for PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM is HOX.

Related Clinical Trials

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.

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Other records listing Neuroscientific Corp. 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.

K880773THE VENUS SYSTEM

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.K881059MCT 8000 (MULTI-VISION CONTRAST TESTER)Vistech Consultants, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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