Clearance Summary
BLOOD LEVEL DETECTOR-MODEL 7601 received FDA 510(k) clearance under submission number K781330, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1978-08-31.
- Submission: K781330
- Applicant / Sponsor: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1978-08-31
Classification & Regulation
This clearance is catalogued under FDA product code FJF and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.