Clearance Summary
ALLIANCE 2690 SEPARATIONS MODULE received FDA 510(k) clearance under submission number K961557, sponsored by Waters Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1996-07-05.
- Submission: K961557
- Applicant / Sponsor: Waters Corporation
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2260
- Decision date: 1996-07-05
Classification & Regulation
This clearance is catalogued under FDA product code LDM and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.