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FDA 510(k)

CARRIAZO BARRAQUER II MICROKERATOME

K-Number: K002191 · 2000-10-12

ApplicantMoria, Inc.
Decision Date2000-10-12
Product CodeHMY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CARRIAZO BARRAQUER II MICROKERATOME is the device name listed in this FDA 510(k) record. The listed applicant is Moria, Inc.. It received FDA 510(k) clearance on 2000-10-12 under 510(k) number K002191. The device is classified under product code HMY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARRIAZO BARRAQUER II MICROKERATOME?

CARRIAZO BARRAQUER II MICROKERATOME is a medical device that received FDA 510(k) clearance on 2000-10-12. The listed applicant is Moria, Inc.. The 510(k) number is K002191.

When did CARRIAZO BARRAQUER II MICROKERATOME receive FDA 510(k) clearance?

CARRIAZO BARRAQUER II MICROKERATOME received FDA 510(k) clearance on 2000-10-12, under 510(k) number K002191.

Who is the listed applicant for CARRIAZO BARRAQUER II 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 II MICROKERATOME?

The FDA product code for CARRIAZO BARRAQUER II 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

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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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