Clearance Summary
DLM112 DAYLINK MONITOR received FDA 510(k) clearance under submission number K062304, sponsored by Rtx Healthcare A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-09-29.
- Submission: K062304
- Applicant / Sponsor: Rtx Healthcare A/S
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2006-09-29
Classification & Regulation
This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.