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FDA 510(k)

AUTOMATED PERIMETERS

K-Number: K803159 · 1981-02-04

ApplicantCoburn Optical Ind., Inc.
Decision Date1981-02-04
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOMATED PERIMETERS is the device name listed in this FDA 510(k) record. The listed applicant is Coburn Optical Ind., Inc.. It received FDA 510(k) clearance on 1981-02-04 under 510(k) number K803159. 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 AUTOMATED PERIMETERS?

AUTOMATED PERIMETERS is a medical device that received FDA 510(k) clearance on 1981-02-04. The listed applicant is Coburn Optical Ind., Inc.. The 510(k) number is K803159.

When did AUTOMATED PERIMETERS receive FDA 510(k) clearance?

AUTOMATED PERIMETERS received FDA 510(k) clearance on 1981-02-04, under 510(k) number K803159.

Who is the listed applicant for AUTOMATED PERIMETERS?

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

What is the FDA product code for AUTOMATED PERIMETERS?

The FDA product code for AUTOMATED PERIMETERS is HPT.

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Other records listing Coburn Optical Ind., 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.

K892347MAGNILINK SYSTEM 101K892351MAGNILINK SYSTEM 602K892349MAGNILINK SYSTEM 209K892348MAGNILINK SYSTEM 201K892350MAGNILINK SYSTEM 402/5K862188IRRIGATION & ASPIRATION/VITRECTOMY DEVICE

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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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