Clearance Summary
MODIFICATION OF APEXPRO TELEMETRY SYSTEM received FDA 510(k) clearance under submission number K021325, sponsored by General Electric Medical Systems Information Techn. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-05-07.
- Submission: K021325
- Applicant / Sponsor: General Electric Medical Systems Information Techn
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2002-05-07
Classification & Regulation
This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.