Clearance Summary
IN VITRO DIAGNOSTIC REAGENT received FDA 510(k) clearance under submission number K772096, sponsored by Pcl-Ria, Inc.. 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 1977-11-22.
- Submission: K772096
- Applicant / Sponsor: Pcl-Ria, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1700
- Decision date: 1977-11-22
Classification & Regulation
This clearance is catalogued under FDA product code CDX and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.