Clearance Summary
GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR received FDA 510(k) clearance under submission number K043352, sponsored by Gocanning Technology , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-03-31.
- Submission: K043352
- Applicant / Sponsor: Gocanning Technology , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2005-03-31
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.