Siemens Burdick, Inc.
Siemens Burdick, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 9, 1992.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K915327 | ELITE II ELECTROCARDIOGRAPH,MODIFIED | October 9, 1992 |
| K915225 | MEGACART | July 1, 1992 |
| K915202 | INTERNAL MODEM FOR THE E560 ELECTROCARDIOGRAPH | May 15, 1992 |
| K914969 | E350I ELECTROCARDIOGRAPH | March 26, 1992 |
| K913518 | TA620 TREADMILL CONTROLLER | October 24, 1991 |
| K910634 | DC200 DEFIBRILLATOR | July 24, 1991 |
| K910867 | T600 TREADMILL | May 31, 1991 |