510(k) K901474
K901474 is an FDA 510(k) premarket notification submitted by Siemens Life Support Systems for the device "ANESTHESIA WORKSTATION". The FDA issued a decision of Substantially Equivalent on April 10, 1990. The device falls under product code BRY (Cabinet, Table And Tray, Anesthesia), a Class I device regulated under 21 CFR 868.6100. Siemens Life Support Systems has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 10, 1990
- Date Received
- March 27, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cabinet, Table And Tray, Anesthesia
- Device Class
- Class I
- Regulation Number
- 868.6100
- Review Panel
- AN
- Submission Type