Asia-Med GmbH and CO KG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Asia-Med GmbH and CO KG has 4 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 4 cleared submissions from 2001 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Asia-Med GmbH and CO KG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Asia-Med GmbH and CO KG
4 devices
Cleared
Dec 02, 2013
CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE...
General Hospital
77d
Cleared
Oct 14, 2005
STANDARD, SPECIAL, SPECIAL+, SNEEDLE B-TYPE AND SNEEDLE J-TYPE ACUPUNCTURE...
General Hospital
73d
Cleared
Jul 10, 2003
SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE
General Hospital
37d
Cleared
Jul 10, 2001
ASIA-MED ACUPUNCTURE NEEDLES, (STANDARD, SPECIAL, COMPACT, APEX)
General Hospital
29d