Clearance Summary
STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE received FDA 510(k) clearance under submission number K950990, sponsored by Stoeckert Instrumente. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-01-19.
- Submission: K950990
- Applicant / Sponsor: Stoeckert Instrumente
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4220
- Decision date: 1996-01-19
Classification & Regulation
This clearance is catalogued under FDA product code DTQ and 21 CFR 870.4220, within the Cardiovascular review panel as a Class II device.