Clearance Summary
MMH PTH RIA KIT received FDA 510(k) clearance under submission number K830700, sponsored by Diagnostic Systems. 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 1983-04-06.
- Submission: K830700
- Applicant / Sponsor: Diagnostic Systems
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1545
- Decision date: 1983-04-06
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.