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FDA 510(k)

MS-30 AUTOMATIC PERIMETER

K-Number: K943234 · 1994-07-27

ApplicantMarco Ophthalmic, Inc.
Decision Date1994-07-27
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MS-30 AUTOMATIC PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Marco Ophthalmic, Inc.. It received FDA 510(k) clearance on 1994-07-27 under 510(k) number K943234. 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 MS-30 AUTOMATIC PERIMETER?

MS-30 AUTOMATIC PERIMETER is a medical device that received FDA 510(k) clearance on 1994-07-27. The listed applicant is Marco Ophthalmic, Inc.. The 510(k) number is K943234.

When did MS-30 AUTOMATIC PERIMETER receive FDA 510(k) clearance?

MS-30 AUTOMATIC PERIMETER received FDA 510(k) clearance on 1994-07-27, under 510(k) number K943234.

Who is the listed applicant for MS-30 AUTOMATIC PERIMETER?

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

What is the FDA product code for MS-30 AUTOMATIC PERIMETER?

The FDA product code for MS-30 AUTOMATIC PERIMETER is HPT.

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Other records listing Marco Ophthalmic, 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.

K930442MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPSK930437MARCO STANDARD RADIUSGAUGESK930444MARCO STANDARD KERATOMETERSK930438MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPSK930439MARCO SURGISCOPE OPERATION MICROSCOPESK930447MARCO H AND TS-1 INSTRUMENT TABLES

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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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