Clearance Summary
ALBU TROL, LOW, MODEL 108.001.002; ALBU TROL, HIGH 108.002.002 received FDA 510(k) clearance under submission number K060215, sponsored by Eurotrol B.V.. 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 2006-03-24.
- Submission: K060215
- Applicant / Sponsor: Eurotrol B.V.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 2006-03-24
Classification & Regulation
This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.