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FDA 510(k)

METAVISION CLINICAL INFORMATION SYSTEM

K-Number: K012349 · 2002-01-29

ApplicantImdsoft, Ltd.
Decision Date2002-01-29
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

METAVISION CLINICAL INFORMATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Imdsoft, Ltd.. It received FDA 510(k) clearance on 2002-01-29 under 510(k) number K012349. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METAVISION CLINICAL INFORMATION SYSTEM?

METAVISION CLINICAL INFORMATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is Imdsoft, Ltd.. The 510(k) number is K012349.

When did METAVISION CLINICAL INFORMATION SYSTEM receive FDA 510(k) clearance?

METAVISION CLINICAL INFORMATION SYSTEM received FDA 510(k) clearance on 2002-01-29, under 510(k) number K012349.

Who is the listed applicant for METAVISION CLINICAL INFORMATION SYSTEM?

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

What is the FDA product code for METAVISION CLINICAL INFORMATION SYSTEM?

The FDA product code for METAVISION CLINICAL INFORMATION SYSTEM is MWI.

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Related Devices (Code: MWI)

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

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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