EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800
K-Number: K964702 · 1997-05-20
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Device Summary
Frequently Asked Questions
What is the EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800?
EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800 is a medical device that received FDA 510(k) clearance on 1997-05-20. The listed applicant is Euclid Systems Corp.. The 510(k) number is K964702.
When did EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800 receive FDA 510(k) clearance?
EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800 received FDA 510(k) clearance on 1997-05-20, under 510(k) number K964702.
Who is the listed applicant for EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800?
The FDA 510(k) record lists Euclid Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800?
The FDA product code for EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800 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.
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.
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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