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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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