CARRIAZO BARRAQUER SINGLE USE MICROKERATOME
K-Number: K003594 · 2001-03-09
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Device Summary
Frequently Asked Questions
What is the CARRIAZO BARRAQUER SINGLE USE MICROKERATOME?
CARRIAZO BARRAQUER SINGLE USE MICROKERATOME is a medical device that received FDA 510(k) clearance on 2001-03-09. The listed applicant is Moria, Inc.. The 510(k) number is K003594.
When did CARRIAZO BARRAQUER SINGLE USE MICROKERATOME receive FDA 510(k) clearance?
CARRIAZO BARRAQUER SINGLE USE MICROKERATOME received FDA 510(k) clearance on 2001-03-09, under 510(k) number K003594.
Who is the listed applicant for CARRIAZO BARRAQUER SINGLE USE MICROKERATOME?
The FDA 510(k) record lists Moria, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARRIAZO BARRAQUER SINGLE USE MICROKERATOME?
The FDA product code for CARRIAZO BARRAQUER SINGLE USE MICROKERATOME is HMY.
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.
Other records listing Moria, 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.
Related Devices (Code: HMY)
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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