Clearance Summary
ESTECH PERCUTANEOUS INSERTION DILATOR KIT received FDA 510(k) clearance under submission number K070749, sponsored by Coombs Medical Device Consulting. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-10-24.
- Submission: K070749
- Applicant / Sponsor: Coombs Medical Device Consulting
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1310
- Decision date: 2007-10-24
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.