Clearance Summary
PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX received FDA 510(k) clearance under submission number K901141, sponsored by Baxter Healthcare Corp. 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 1990-04-09.
- Submission: K901141
- Applicant / Sponsor: Baxter Healthcare Corp
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2150
- Decision date: 1990-04-09
Classification & Regulation
This clearance is catalogued under FDA product code JJC and 21 CFR 862.2150, within the Clinical Chemistry review panel as a Class I device.