Clearance Summary
IMMULITE/IMMULITE 1000 TURBO INTACT PTH received FDA 510(k) clearance under submission number K053533, sponsored by Diagnostic Products 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 2006-02-03.
- Submission: K053533
- Applicant / Sponsor: Diagnostic Products Corporation
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1545
- Decision date: 2006-02-03
Classification & Regulation
This clearance is catalogued under FDA product code CEW and 21 CFR 862.1545, within the Clinical Chemistry review panel as a Class II device.