Clearance Summary
SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE received FDA 510(k) clearance under submission number K873533, sponsored by Medical Electronics Laboratories, 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 1988-01-29.
- Submission: K873533
- Applicant / Sponsor: Medical Electronics Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 1988-01-29
Classification & Regulation
This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.