Siemens Medical Electronics
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K935043 | SIEMENS CLINICAL WORK STATION | April 7, 1995 |
| K921930 | SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI | May 7, 1993 |
| K920445 | SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIES | March 2, 1993 |
| K914765 | SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYS | November 6, 1992 |
| K912070 | SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT | April 23, 1992 |
| K913489 | SIEMENS MICRO2 PULSE OXIMETER | October 30, 1991 |
| K905775 | SIEMENS ETCO2 CARTRIDGE | March 11, 1991 |
| K900319 | SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM | June 28, 1990 |
| K901771 | SIEMENS SIRECUST 732, PATIENT MONITOR | May 30, 1990 |
| K894460 | SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA | October 2, 1989 |
| K891481 | SIEMENS SIRECUST TRANSCUTANEOUS CARBON DIOXIDE | September 29, 1989 |
| K893470 | SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE | August 3, 1989 |
| K891023 | SIEMENS CEILING STAND 800F, 800 AND 810 | July 25, 1989 |
| K890791 | SIEMENS SIRECUST 730 PATIENT MONITOR | May 2, 1989 |
| K881939 | SIRECUST 1280/1281 & 960/961 PATIENT MONITORS | July 18, 1988 |