Clearance Summary
DEFIBRILLATOR ANALYZER - DA-2006P received FDA 510(k) clearance under submission number K110192, sponsored by Bc Group International, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-02-08.
- Submission: K110192
- Applicant / Sponsor: Bc Group International, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5325
- Decision date: 2011-02-08
Classification & Regulation
This clearance is catalogued under FDA product code DRL and 21 CFR 870.5325, within the Cardiovascular review panel as a Class II device.