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FDA 510(k)

EH-270 CORNEAL TOPOGRAPHER

K-Number: K933556 · 1993-11-02

ApplicantVisioptic, Inc.
Decision Date1993-11-02
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EH-270 CORNEAL TOPOGRAPHER is the device name listed in this FDA 510(k) record. The listed applicant is Visioptic, Inc.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K933556. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EH-270 CORNEAL TOPOGRAPHER?

EH-270 CORNEAL TOPOGRAPHER is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Visioptic, Inc.. The 510(k) number is K933556.

When did EH-270 CORNEAL TOPOGRAPHER receive FDA 510(k) clearance?

EH-270 CORNEAL TOPOGRAPHER received FDA 510(k) clearance on 1993-11-02, under 510(k) number K933556.

Who is the listed applicant for EH-270 CORNEAL TOPOGRAPHER?

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

What is the FDA product code for EH-270 CORNEAL TOPOGRAPHER?

The FDA product code for EH-270 CORNEAL TOPOGRAPHER is HLQ.

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Related Devices (Code: HLQ)

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.

K003299OPD-SCAN, MODELS ARK-10000 AND ARK-9000Nidek Co., Ltd.K973756EYE SYS VISTAEyesys Technologies, Inc.K964290EYECHEKReichert Ophthalmic Instruments, Div. Leica, Inc.K945382TECHNOMED C-SCAN COLOR ELLIPSOID TOPOMETERExpertech Assoc., Inc.K944207TOPOGRAPHIC MODELING SYSTEM 2 TMS-2Computed Anatomy, Inc.K944616KERATRON CORNEAL TOPOGRAPHERAlliance Medical Marketinig

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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