Clearance Summary
AMERLEX-M PROGESTERONE RADIOIMMUNOASSAY KIT CODE received FDA 510(k) clearance under submission number K845026, sponsored by Amersham 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 1985-02-01.
- Submission: K845026
- Applicant / Sponsor: Amersham Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1620
- Decision date: 1985-02-01
Classification & Regulation
This clearance is catalogued under FDA product code JLS and 21 CFR 862.1620, within the Clinical Chemistry review panel as a Class I device.