Clearance Summary
FASTPACK TESTO IMMUNOASSAY received FDA 510(k) clearance under submission number K101388, sponsored by Qualigen, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2011-02-18.
- Submission: K101388
- Applicant / Sponsor: Qualigen, Inc.
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1680
- Decision date: 2011-02-18
Classification & Regulation
This clearance is catalogued under FDA product code CDZ and 21 CFR 862.1680, within the Clinical Chemistry review panel as a Class I device.