Deka Research & Development Corp.
Country not established FDA establishment FEI 1220973
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
What Deka Research & Development Corp. makes
DEKA Research & Development Corp. manufactures a range of medical devices including volumetric infusion controllers, automated peritoneal dialysis systems, peristaltic pumps for treprostinil injection, and advanced mobility platforms such as the iBOT and TAC device, as well as related administration sets and system accessories.
All of these products are classified as Class II medical devices and are listed in the FDA 510(k) database; the company is based in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 1220973
- Address
- 340 Commercial St, Manchester, NH, 03101
Frequently asked questions
How many devices does DEKA RESEARCH & DEVELOPMENT CORP. have in the registry?
The registry currently lists 11 devices for DEKA RESEARCH & DEVELOPMENT CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list DEKA RESEARCH & DEVELOPMENT CORP.'s devices?
Among its 11 most recently registered devices, DEKA RESEARCH & DEVELOPMENT CORP. has devices listed in FDA 510(k) (11 devices).
What risk classes do DEKA RESEARCH & DEVELOPMENT CORP.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for DEKA RESEARCH & DEVELOPMENT CORP.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DEKA RESEARCH & DEVELOPMENT CORP. in the registry?
The most recently registered devices listed for DEKA RESEARCH & DEVELOPMENT CORP. include DK*300 VOLUMETRIC INFUSION CONTROLLER, AMIA AUTOMATED PD SYSTEM, Remunity System and DEKA JR..