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FDA 510(k)

MEDIQ VERSION 1.0

K-Number: K052963 · 2005-12-05

ApplicantClario Medical Imaging, Inc.
Decision Date2005-12-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDIQ VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Clario Medical Imaging, Inc.. It received FDA 510(k) clearance on 2005-12-05 under 510(k) number K052963. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIQ VERSION 1.0?

MEDIQ VERSION 1.0 is a medical device that received FDA 510(k) clearance on 2005-12-05. The listed applicant is Clario Medical Imaging, Inc.. The 510(k) number is K052963.

When did MEDIQ VERSION 1.0 receive FDA 510(k) clearance?

MEDIQ VERSION 1.0 received FDA 510(k) clearance on 2005-12-05, under 510(k) number K052963.

Who is the listed applicant for MEDIQ VERSION 1.0?

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

What is the FDA product code for MEDIQ VERSION 1.0?

The FDA product code for MEDIQ VERSION 1.0 is LLZ.

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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Other records listing Clario Medical Imaging, 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.

K080196Z3D CONTRAST ACUITY

Related Devices (Code: LLZ)

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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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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