Clearance Summary
BOWEN REUSEABLE/DISPOSABLE ELECTRODE received FDA 510(k) clearance under submission number K871325, sponsored by Bowen & Company, 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 1987-06-08.
- Submission: K871325
- Applicant / Sponsor: Bowen & Company, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2360
- Decision date: 1987-06-08
Classification & Regulation
This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.