Clearance Summary
BYRD DILATOR SHEATH SET - TEFLON received FDA 510(k) clearance under submission number K902469, sponsored by Medical Engineering and Development Institute. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-08-23.
- Submission: K902469
- Applicant / Sponsor: Medical Engineering and Development Institute
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1310
- Decision date: 1990-08-23
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.