Clearance Summary
SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR received FDA 510(k) clearance under submission number K863042, sponsored by Siemens Medical Solutions USA, 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 1987-01-14.
- Submission: K863042
- Applicant / Sponsor: Siemens Medical Solutions USA, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1110
- Decision date: 1987-01-14
Classification & Regulation
This clearance is catalogued under FDA product code DSK and 21 CFR 870.1110, within the Cardiovascular review panel as a Class II device.