Clearance Summary
ANGELTOUCH VENTED IV ADMINISTRATION SET received FDA 510(k) clearance under submission number K012189, sponsored by Angiplast Private , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2002-03-05.
- Submission: K012189
- Applicant / Sponsor: Angiplast Private , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 2002-03-05
Classification & Regulation
This clearance is catalogued under FDA product code LHI and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.