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FDA 510(k)

NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT

K-Number: K021231 · 2002-07-30

ApplicantMatritech, Inc.
Decision Date2002-07-30
Product CodeMMW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Matritech, Inc.. It received FDA 510(k) clearance on 2002-07-30 under 510(k) number K021231. The device is classified under product code MMW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT?

NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT is a medical device that received FDA 510(k) clearance on 2002-07-30. The listed applicant is Matritech, Inc.. The 510(k) number is K021231.

When did NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT receive FDA 510(k) clearance?

NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT received FDA 510(k) clearance on 2002-07-30, under 510(k) number K021231.

Who is the listed applicant for NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT?

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

What is the FDA product code for NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT?

The FDA product code for NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT is MMW.

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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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