Medical Device Manufacturer · US , Newton , MA

Matritech, Inc.

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Matritech, Inc. — FDA 510(k) Submissions

Matritech, Inc. has submitted 1 FDA 510(k) premarket notifications since 2002, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Tumor Marker, Monitoring, Bladder . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT

K021231 · MMW System, Test, Tumor... · Immunology

Jul 2002 103d

Matritech, Inc.

Matritech, Inc. — FDA 510(k) Submissions

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