Clearance Summary
MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK received FDA 510(k) clearance under submission number K875325, sponsored by Schneider-Shilley (Usa). The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-02-18.
- Submission: K875325
- Applicant / Sponsor: Schneider-Shilley (Usa)
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1200
- Decision date: 1988-02-18
Classification & Regulation
This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.