FDA 510(k) Applications Submitted by DEKA RESEARCH & DEVELOPMENT CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093915 | 12/22/2009 | DEKA TAC DEVICE | DEKA RESEARCH & DEVELOPMENT CORP. |
| K103220 | 11/01/2010 | VOYAGER PERITONEAL DIALYSIS SYSTEM | DEKA RESEARCH & DEVELOPMENT CORP. |
| K124018 | 12/27/2012 | AMIA AUTOMATED PD SYSTEM | DEKA RESEARCH & DEVELOPMENT CORP. |
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