Clearance Summary
AUTOPULSE RESUSCITATION SYSTEM MODEL 1000 received FDA 510(k) clearance under submission number K112998, sponsored by Zoll Circulation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-03-15.
- Submission: K112998
- Applicant / Sponsor: Zoll Circulation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5200
- Decision date: 2012-03-15
Classification & Regulation
This clearance is catalogued under FDA product code DRM and 21 CFR 870.5200, within the Cardiovascular review panel as a Class II device.