Clearance Summary
DP240 240 HOUR DOPPLER PROBE received FDA 510(k) clearance under submission number K052989, sponsored by Deltex Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-03-08.
- Submission: K052989
- Applicant / Sponsor: Deltex Medical
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2120
- Decision date: 2006-03-08
Classification & Regulation
This clearance is catalogued under FDA product code DPT and 21 CFR 870.2120, within the Cardiovascular review panel as a Class II device.