FDA 510(k) Applications Submitted by Casey Coombs
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162900 | 10/17/2016 | PowerMidline Catheter | C.R. Bard, Inc. |
| K153280 | 11/12/2015 | PowerGlide Pro Midline Catheter | C.R. BARD, INC. |
| K153298 | 11/13/2015 | AccuCath Intravascular Catheter | C.R. Bard, Inc. |
| K153393 | 11/24/2015 | PowerMidline Catheter | C.R. BARD, INC |
| K133856 | 12/19/2013 | POWERGLIDE MIDLINE CATHETER | C.R. BARD, INC. |
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