Clearance Summary
ANS 2000 ECG MONITOR AND RESPIRATION PACER received FDA 510(k) clearance under submission number K973426, sponsored by D. E. Hokanson, 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 1998-08-12.
- Submission: K973426
- Applicant / Sponsor: D. E. Hokanson, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2340
- Decision date: 1998-08-12
Classification & Regulation
This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.