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FDA 510(k)

CORNEAL TOPOGRAPHER 200

K-Number: K963762 · 1996-12-23

ApplicantEclipse Ventures
Decision Date1996-12-23
Product CodeMMQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CORNEAL TOPOGRAPHER 200 is the device name listed in this FDA 510(k) record. The listed applicant is Eclipse Ventures. It received FDA 510(k) clearance on 1996-12-23 under 510(k) number K963762. The device is classified under product code MMQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNEAL TOPOGRAPHER 200?

CORNEAL TOPOGRAPHER 200 is a medical device that received FDA 510(k) clearance on 1996-12-23. The listed applicant is Eclipse Ventures. The 510(k) number is K963762.

When did CORNEAL TOPOGRAPHER 200 receive FDA 510(k) clearance?

CORNEAL TOPOGRAPHER 200 received FDA 510(k) clearance on 1996-12-23, under 510(k) number K963762.

Who is the listed applicant for CORNEAL TOPOGRAPHER 200?

The FDA 510(k) record lists Eclipse Ventures as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORNEAL TOPOGRAPHER 200?

The FDA product code for CORNEAL TOPOGRAPHER 200 is MMQ.

Related Clinical Trials

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.

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Related Devices (Code: MMQ)

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.

K981665SILON TOPOMAT CORNEAL TOPOGRAPHY IMAGE ENHANCEMENT DEVICEBio-Medical Sciences, Inc.K964702EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800Euclid Systems Corp.K964891ORBSHOT KERATOMETEROrbtek, Inc.K950077INTRAOPERATIVE CORNEAL TOPOGRAPHY SYSTEM (I-CTS)Par Vision Systems Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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