Carmel Pharma Ab. is one of 135 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Carmel Pharma Ab. - FDA 510(k) Cleared Devices
Recent clearances: INFUSION ADAPTER C100, INJECTOR LUER, MODEL N34, INJECTOR LUER LOCK, MODEL N35, INJECTOR LUER LOCK, N35C, CONNECTOR LUER LOCK, MODEL C35,, PHASEAL PROTECTOR P14, P21, P28 AND P50
7
Total
7
Cleared
0
Denied
Carmel Pharma Ab. has 7 FDA 510(k) cleared medical devices. Based in Gothenburg, SE.
Historical record: 7 cleared submissions from 1998 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Carmel Pharma Ab. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carmel Pharma Ab.
7 devices
Cleared
Apr 12, 2011
INFUSION ADAPTER C100
General Hospital
99d
Cleared
Dec 07, 2009
INJECTOR LUER, MODEL N34, INJECTOR LUER LOCK, MODEL N35, INJECTOR LUER LOCK,...
General Hospital
88d
Cleared
Mar 23, 2009
PHASEAL PROTECTOR P14, P21, P28 AND P50
General Hospital
14d
Cleared
Apr 28, 2006
PHASEAL - CLOSED SYSTEM FOR THE PREPARATION AND ADMINISTRATION OF PARENTERAL...
General Hospital
29d
Cleared
Nov 15, 2002
PHASEAL
General Hospital
7d
Cleared
May 12, 2000
PROTECTOR 21, PROTECTOR 50, PROTECTOR 14, INJECTOR LUER LOCK, INFUSION ADAPTER
General Hospital
11d
Cleared
Mar 03, 1998
PHASEAL, CLOSED SYSTEM FORHANDLING OF PARENTERAL DRUGS, ADDITIONAL...
General Hospital
29d