Clearance Summary
PowerLoc MAX Power-Injectable Infusion Set and SafeStep Huber Needle Set received FDA 510(k) clearance under submission number K171735, sponsored by C.R. Bard, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2017-08-08.
- Submission: K171735
- Applicant / Sponsor: C.R. Bard, Inc.
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 2017-08-08
Classification & Regulation
This clearance is catalogued under FDA product code PTI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.