Clearance Summary
SILICONE OIL 350 CNETISTOKE received FDA 510(k) clearance under submission number K854273, sponsored by Pacific Medical Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-11-22.
- Submission: K854273
- Applicant / Sponsor: Pacific Medical Industries
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3300
- Decision date: 1985-11-22
Classification & Regulation
This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.