Amco International Manufacturing & Design, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amco International Manufacturing & Design, Inc. - FDA 510(k) Cleared ...
5
Total
5
Cleared
0
Denied
Amco International Manufacturing & Design, Inc. has 5 FDA 510(k) cleared medical devices. Based in Elizabeth, US.
Historical record: 5 cleared submissions from 2007 to 2009. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Amco International Manufacturing & Design, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amco International Manufacturing & Design, Inc.
5 devices
Cleared
Aug 07, 2009
AMCO REPLACEMENT BATTERY FOR PHILIPS MEDICAL MODELS BT1 AND M5070A
Cardiovascular
72d
Cleared
Nov 25, 2008
AMCO REPLACEMENT BATTERY FOR POWERHEART AED, NON-RECHARGEABLE, MODEL 2L561
Cardiovascular
57d
Cleared
Apr 11, 2008
LIFE+CEL OR LIFECEL BATTERY
Cardiovascular
102d
Cleared
Jan 24, 2008
LIFE+CEL OR LIFECEL BATTERY PACK, MODEL 5L500
Cardiovascular
132d
Cleared
Dec 07, 2007
LIFE+CEL BATTERY
Cardiovascular
225d