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FDA 510(k)

MARCO PROJECTION PERIMETER

K-Number: K930448 · 1993-06-21

ApplicantMarco Ophthalmic, Inc.
Decision Date1993-06-21
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARCO PROJECTION 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 1993-06-21 under 510(k) number K930448. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARCO PROJECTION PERIMETER?

MARCO PROJECTION PERIMETER is a medical device that received FDA 510(k) clearance on 1993-06-21. The listed applicant is Marco Ophthalmic, Inc.. The 510(k) number is K930448.

When did MARCO PROJECTION PERIMETER receive FDA 510(k) clearance?

MARCO PROJECTION PERIMETER received FDA 510(k) clearance on 1993-06-21, under 510(k) number K930448.

Who is the listed applicant for MARCO PROJECTION 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 MARCO PROJECTION PERIMETER?

The FDA product code for MARCO PROJECTION PERIMETER is HOO.

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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.

K943234MS-30 AUTOMATIC PERIMETERK930437MARCO STANDARD RADIUSGAUGESK930444MARCO STANDARD KERATOMETERSK930438MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPSK930442MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPSK930439MARCO SURGISCOPE OPERATION MICROSCOPES

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Related Devices (Code: HOO)

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.

K941723WELCH ALLYN GLAUCOMA DETECTORWelch Allyn, Inc.K873912RICHMOND VISUAL FIELD SCREENERRichmond Products, Inc.K864467HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREENKeeler Instruments, Inc.K860115DIGILAB CAMBRIDGE PERIMETERBio-RadK832800AUTOMATIC TANGENT SCREEN 50CooperVision, 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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