Clearance Summary
HRT SERIES 100 ELECTROPHYSIOLOGY CATHETER received FDA 510(k) clearance under submission number K932388, sponsored by Heart Rhythm Technologies, 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 1995-05-31.
- Submission: K932388
- Applicant / Sponsor: Heart Rhythm Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1220
- Decision date: 1995-05-31
Classification & Regulation
This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.