Company ยท US
Fluke Biomedical
FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2013. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 25, 2013 | K121860 | ESA615 Fluke Biomedical | DRT |
| Oct 11, 2012 | K121722 | ESA620 ELECTRICAL SAFETY ANALYZER Fluke Biomedical | DRT |
| Sep 2, 2011 | K110429 | PROSIM 4, PROSIM 6, PROSIM 8 Fluke Biomedical | DRT |
| Apr 13, 2011 | K103336 | MPS450 MULTIPARAMETER SIMULATOR Fluke Biomedical | DRT |
| Dec 24, 2008 | K083347 | IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADS Fluke Biomedical | DRL |
| Jan 28, 2008 | K072114 | IMPULSE 6000D/7000DP Fluke Biomedical | DRL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||