Clearance Summary
FIBROSYSTEM received FDA 510(k) clearance under submission number K823520, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1982-12-28.
- Submission: K823520
- Applicant / Sponsor: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.7900
- Decision date: 1982-12-28
Classification & Regulation
This clearance is catalogued under FDA product code GKQ and 21 CFR 864.7900, within the Hematology review panel as a Class I device.