Clearance Summary
SIEMENS CEILING STAND 800F, 800 AND 810 received FDA 510(k) clearance under submission number K891023, sponsored by Siemens Medical Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-07-25.
- Submission: K891023
- Applicant / Sponsor: Siemens Medical Electronics
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1989-07-25
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.