Clearance Summary
JOSTRA FLOWPROBE FP-32E received FDA 510(k) clearance under submission number K013939, sponsored by Jostra AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-12-14.
- Submission: K013939
- Applicant / Sponsor: Jostra AG
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2120
- Decision date: 2001-12-14
Classification & Regulation
This clearance is catalogued under FDA product code DPT and 21 CFR 870.2120, within the Cardiovascular review panel as a Class II device.