Clearance Summary
HDL EX-SEP PRECIPITATING REAGENT received FDA 510(k) clearance under submission number K833431, sponsored by Preventive Diagnostics 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 1984-01-13.
- Submission: K833431
- Applicant / Sponsor: Preventive Diagnostics Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1475
- Decision date: 1984-01-13
Classification & Regulation
This clearance is catalogued under FDA product code LBR and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.