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FDA 510(k)

MICROWARE 200

K-Number: K050740 · 2005-04-06

ApplicantMicroware, Inc.
Decision Date2005-04-06
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICROWARE 200 is the device name listed in this FDA 510(k) record. The listed applicant is Microware, Inc.. It received FDA 510(k) clearance on 2005-04-06 under 510(k) number K050740. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROWARE 200?

MICROWARE 200 is a medical device that received FDA 510(k) clearance on 2005-04-06. The listed applicant is Microware, Inc.. The 510(k) number is K050740.

When did MICROWARE 200 receive FDA 510(k) clearance?

MICROWARE 200 received FDA 510(k) clearance on 2005-04-06, under 510(k) number K050740.

Who is the listed applicant for MICROWARE 200?

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

What is the FDA product code for MICROWARE 200?

The FDA product code for MICROWARE 200 is GZJ.

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Related Devices (Code: GZJ)

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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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