Clearance Summary
TERUMO SENSIBEAD EIA HGH KIT received FDA 510(k) clearance under submission number K852299, sponsored by Terumo Medical 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 1985-07-09.
- Submission: K852299
- Applicant / Sponsor: Terumo Medical Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1370
- Decision date: 1985-07-09
Classification & Regulation
This clearance is catalogued under FDA product code CFL and 21 CFR 862.1370, within the Clinical Chemistry review panel as a Class I device.