Clearance Summary
Caretaker Remote Display App and Caretaker Software Library received FDA 510(k) clearance under submission number K181196, sponsored by Caretaker Medical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-10-03.
- Submission: K181196
- Applicant / Sponsor: Caretaker Medical, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2018-10-03
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.