Medfusion, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medfusion, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medfusion, Inc. has 5 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 5 cleared submissions from 1989 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medfusion, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medfusion, Inc.
5 devices
Cleared
Jan 11, 1991
MODIFIED WALKMED 400
General Hospital
24d
Cleared
Dec 24, 1990
MODEL 2001, MODIFICATION
General Hospital
54d
Cleared
Aug 29, 1990
MODEL 3001 SYRINGE INFUSION PUMP
General Hospital
134d
Cleared
Aug 03, 1989
AMBULATORY INFUSION PUMP
General Hospital
163d
Cleared
Jul 27, 1989
SYRINGE INFUSION PUMP
General Hospital
197d