Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
1 active
Filters
1 active
Registry
EUDAMED
FDA 510(k)
11
FDA PMA
GUDID
Country / market
United States
11
Risk class
Class I
Class IIa
Class IIb
Class III
Class II (US)
11
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Validated only
Category (EMDN)
Browse by category
Apply filters
Reset
11 devices found
·
sorted by relevance
Key
Manufacturer: Deka Research & Development Corp.
×
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
DK*300 Volumetric Infusion Controller
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K843254
Active
Cleared 11 Oct 1984
Active
510(k)
510(k)
II
Amia Automated Pd System
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K124018
Active
Cleared 14 Jun 2013
Active
510(k)
510(k)
II
Remunity System
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K243354
Active
Cleared 27 Nov 2024
Active
510(k)
510(k)
II
Deka Jr.
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K863204
Active
Cleared 3 Sep 1986
Active
510(k)
510(k)
II
RemunityPRO™ Pump for Remodulin® (treprostinil) Injection
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K250357
Active
Cleared 11 Mar 2025
Active
510(k)
510(k)
II
Voyager Peritoneal Dialysis System
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K103220
Active
Cleared 29 Jul 2011
Active
510(k)
510(k)
II
twiist system
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K250930
Active
Cleared 2 Apr 2025
Active
510(k)
510(k)
II
Next Generation iBOT
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K172601
Active
Cleared 2 Mar 2018
Active
510(k)
510(k)
II
Deka Tac Device
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K093915
Active
Cleared 23 Aug 2011
Active
510(k)
510(k)
II
Deka Solution Admin. Set Dk 302-A
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K843054
Active
Cleared 13 Sep 1984
Active
510(k)
510(k)
II
Remunity 2.0 Pump for Remodulin (treprostinil) Injection
Deka Research & Development Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K241736
Active
Cleared 16 Jan 2025
Active
510(k)
510(k)
II
Previous
Next
Showing 1-11 of 11