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FDA 510(k)

AUTOMATIC PERIMETER, AP-340

K-Number: K881219 · 1988-05-03

ApplicantKowa Optimed, Inc.
Decision Date1988-05-03
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC PERIMETER, AP-340 is the device name listed in this FDA 510(k) record. The listed applicant is Kowa Optimed, Inc.. It received FDA 510(k) clearance on 1988-05-03 under 510(k) number K881219. 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 AUTOMATIC PERIMETER, AP-340?

AUTOMATIC PERIMETER, AP-340 is a medical device that received FDA 510(k) clearance on 1988-05-03. The listed applicant is Kowa Optimed, Inc.. The 510(k) number is K881219.

When did AUTOMATIC PERIMETER, AP-340 receive FDA 510(k) clearance?

AUTOMATIC PERIMETER, AP-340 received FDA 510(k) clearance on 1988-05-03, under 510(k) number K881219.

Who is the listed applicant for AUTOMATIC PERIMETER, AP-340?

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

What is the FDA product code for AUTOMATIC PERIMETER, AP-340?

The FDA product code for AUTOMATIC PERIMETER, AP-340 is HPT.

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Other records listing Kowa Optimed, 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.

K013805KOWA AUTOMATED TONOMETER KT-500K961090AUTOMATIC VISUAL FIELD PLOTTER AP-125K960924KOWA HAND-HELD APPLANATION TONOMETER HA-1K955442KOWA SC-1200 PHOTO SLIT LAMP SYSTEMK954781KOWA GENESIS HAND-HELD FUNDUS CAMERAK954780KOWA PROFESSIONAL FUNDUS CAMERA MODELS FX-500, FX-500S, FX-500C

View all 10 devices →

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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