Clearance Summary
TRIO MONITOR MODEL 0998-00-0600 received FDA 510(k) clearance under submission number K032338, sponsored by Datascope Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-02-11.
- Submission: K032338
- Applicant / Sponsor: Datascope Corp.
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2004-02-11
Classification & Regulation
This clearance is catalogued under FDA product code MWI and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.