Clearance Summary
ISECURE SYRINGE CARTRIDGE HOLDER received FDA 510(k) clearance under submission number K063180, sponsored by Hospira, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2006-12-11.
- Submission: K063180
- Applicant / Sponsor: Hospira, Inc.
- Clearance pathway: Special
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5050
- Decision date: 2006-12-11
Classification & Regulation
This clearance is catalogued under FDA product code IQG and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.