Deka Research & Development Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deka Research & Development Corp. - FDA 510(k) Cleared Devices
Recent clearances: twiist system, RemunityPRO™ Pump for Remodulin® (treprostinil) Injection, Remunity System
10
Total
10
Cleared
0
Denied
Deka Research & Development Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: Apr 2025. Active since 1984. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Deka Research & Development Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Deka Research & Development Corp.
10 devices
Cleared
Apr 02, 2025
twiist system
Chemistry
5d
Cleared
Mar 11, 2025
RemunityPRO™ Pump for Remodulin® (treprostinil) Injection
General Hospital
32d
Cleared
Nov 27, 2024
Remunity System
General Hospital
29d
Cleared
Mar 02, 2018
Next Generation iBOT
Physical Medicine
184d
Cleared
Jun 14, 2013
AMIA AUTOMATED PD SYSTEM
Gastroenterology & Urology
169d
Cleared
Aug 23, 2011
DEKA TAC DEVICE
Gastroenterology & Urology
609d
Cleared
Jul 29, 2011
VOYAGER PERITONEAL DIALYSIS SYSTEM
Gastroenterology & Urology
270d
Cleared
Sep 03, 1986
DEKA JR.
General Hospital
15d
Cleared
Oct 11, 1984
DK*300 VOLUMETRIC INFUSION CONTROLLER
General Hospital
52d
Cleared
Sep 13, 1984
DEKA SOLUTION ADMIN. SET DK 302-A
General Hospital
41d