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FDA 510(k)

PATTERN DISCRIMINATION PERIMETER

K-Number: K874336 · 1988-01-12

ApplicantLkc Technologies, Inc.
Decision Date1988-01-12
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PATTERN DISCRIMINATION PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lkc Technologies, Inc.. It received FDA 510(k) clearance on 1988-01-12 under 510(k) number K874336. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATTERN DISCRIMINATION PERIMETER?

PATTERN DISCRIMINATION PERIMETER is a medical device that received FDA 510(k) clearance on 1988-01-12. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K874336.

When did PATTERN DISCRIMINATION PERIMETER receive FDA 510(k) clearance?

PATTERN DISCRIMINATION PERIMETER received FDA 510(k) clearance on 1988-01-12, under 510(k) number K874336.

Who is the listed applicant for PATTERN DISCRIMINATION PERIMETER?

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

What is the FDA product code for PATTERN DISCRIMINATION PERIMETER?

The FDA product code for PATTERN DISCRIMINATION PERIMETER is HPT.

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Other records listing Lkc Technologies, 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.

K914163SCOPTOPIC SENSITIVITY TEST-1[SST-1]K913962ANOMALOSCOPE QUADRANT TEST-6K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]K820414UNIVERSAL TESTING & ANALYSIS SYSTEMSK790109TELEMETRY, BIOMEDICALK760199ELECTRORETINOGRAPH

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Related Devices (Code: HPT)

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.

K092187MAIA, MODEL 1Centervue S.P.A.K093213GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIESCarl Zeiss Meditec, Inc.K091579FORESEE HOMENotal Vision , Ltd.K063310TRUEFIELD ANALYZERSeeing Machines LimitedK050350THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)Notal Vision, Inc.K023623NOVAVISION, MODEL 2.0Novavision, 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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