Clearance Summary
CARDIAC TRIGGER, MODEL: CTM300 received FDA 510(k) clearance under submission number K083854, sponsored by Ivy Biomedical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-02-13.
- Submission: K083854
- Applicant / Sponsor: Ivy Biomedical Systems, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2009-02-13
Classification & Regulation
This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.