Carefusion 209, Inc.
Carefusion 209, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 25, 2012.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K120979 | CAREFUSION NICOLET EDX | April 25, 2012 |
| K112052 | CAREFUSION NICOLET EDX | March 15, 2012 |
| K112034 | TECA ELITE DISPOSABLE CONCENTRIC NEEDLES | August 12, 2011 |
| K111131 | TECA (TM) ELITE DISPOSABLE MONOPOLAR NEEDLES | June 17, 2011 |
| K103140 | NICOLET WIRELESS EEG | April 8, 2011 |