Clearance Summary
SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL received FDA 510(k) clearance under submission number K003243, sponsored by Siemens Medical Solutions USA, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-12-21.
- Submission: K003243
- Applicant / Sponsor: Siemens Medical Solutions USA, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2000-12-21
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.