Clearance Summary
SHBG IRMA KIT received FDA 510(k) clearance under submission number K861679, sponsored by Farmos Group , Ltd.. 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 1987-03-13.
- Submission: K861679
- Applicant / Sponsor: Farmos Group , Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1680
- Decision date: 1987-03-13
Classification & Regulation
This clearance is catalogued under FDA product code CDZ and 21 CFR 862.1680, within the Clinical Chemistry review panel as a Class I device.