Clearance Summary
NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT received FDA 510(k) clearance under submission number K021231, sponsored by Matritech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2002-07-30.
- Submission: K021231
- Applicant / Sponsor: Matritech, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.6010
- Decision date: 2002-07-30
Classification & Regulation
This clearance is catalogued under FDA product code MMW and 21 CFR 866.6010, within the Immunology review panel as a Class II device.