Clearance Summary
PERCUTANEOUS ENTRY NEEDLE, SELDINGER received FDA 510(k) clearance under submission number K813461, sponsored by Ocean Medical Products, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-12-29.
- Submission: K813461
- Applicant / Sponsor: Ocean Medical Products, Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1310
- Decision date: 1981-12-29
Classification & Regulation
This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.