Clearance Summary
LIFECARD CF COMPACT RECORDER received FDA 510(k) clearance under submission number K001025, sponsored by Reynolds Medical , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-04-19.
- Submission: K001025
- Applicant / Sponsor: Reynolds Medical , Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2800
- Decision date: 2000-04-19
Classification & Regulation
This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.