Clearance Summary
DIRECT ESTRIOL RIA KIT received FDA 510(k) clearance under submission number K781546, sponsored by Immunalysis 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 1978-12-04.
- Submission: K781546
- Applicant / Sponsor: Immunalysis Corporation
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1265
- Decision date: 1978-12-04
Classification & Regulation
This clearance is catalogued under FDA product code CGI and 21 CFR 862.1265, within the Clinical Chemistry review panel as a Class I device.