Owen Mumford USA, Inc. is one of 15078 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Owen Mumford USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AUTOJET 2 (NON-FIXED NEEDLE TYPE), UNIFINE, OWEN MUMFORD 3ML AUTOPEN
10
Total
10
Cleared
0
Denied
Owen Mumford USA, Inc. has 10 FDA 510(k) cleared general hospital devices. Based in Marietta, US.
Historical record: 10 cleared submissions from 1995 to 2001.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Owen Mumford USA, Inc.
10 devices
Cleared
Nov 13, 2001
AUTOJECT 2
General Hospital
34d
Cleared
Nov 10, 1999
AUTOJET 2 (NON-FIXED NEEDLE TYPE)
General Hospital
33d
Cleared
Jan 08, 1999
UNIFINE
General Hospital
60d
Cleared
Dec 21, 1998
OWEN MUMFORD 3ML AUTOPEN
General Hospital
42d
Cleared
Dec 04, 1998
RAPPORT V.T.D.
Gastroenterology & Urology
158d
Cleared
Nov 25, 1998
AMIELLE
Obstetrics & Gynecology
85d
Cleared
Dec 04, 1997
UNIFINE PENTIPS
General Hospital
51d
Cleared
Sep 26, 1997
RAPPORT V.T.D.
Gastroenterology & Urology
158d
Cleared
Nov 08, 1995
AUTOJECT MINI
General Hospital
90d
Cleared
Aug 11, 1995
AUTOJECT 2
General Hospital
267d