Clearance Summary
AMBULATORY PH RECORDING DEVICE received FDA 510(k) clearance under submission number K842349, sponsored by Clinical Data Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-06-14.
- Submission: K842349
- Applicant / Sponsor: Clinical Data Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2800
- Decision date: 1985-06-14
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.