Clearance Summary
EVICEL APPLICATION DEVICE received FDA 510(k) clearance under submission number K130900, sponsored by Ethicon Inc (On Behalf of Omrix Biopharaceuticals. 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 2013-08-13.
- Submission: K130900
- Applicant / Sponsor: Ethicon Inc (On Behalf of Omrix Biopharaceuticals
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2013-08-13
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.