Medefil, Inc. is one of 20339 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medefil, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDEFLUSH NORMAL SALINE I.V. FLUSH SYRINGE-STERILE FIELD READY, MEDEFIL'S HEPARIN I.V. FLUSH SYRINGE 1 UNIT/ML, MEDEFIL'S NORMAL SALINE I.V. FLUSH SYRINGE
7
Total
7
Cleared
0
Denied
Medefil, Inc. has 7 FDA 510(k) cleared medical devices. Based in Schaumburg, US.
Historical record: 7 cleared submissions from 2000 to 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medefil, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medefil, Inc.
7 devices
Cleared
Sep 20, 2012
MEDEFLUSH NORMAL SALINE I.V. FLUSH SYRINGE-STERILE FIELD READY
General Hospital
147d
Cleared
Feb 03, 2010
MEDEFIL'S HEPARIN I.V. FLUSH SYRINGE 1 UNIT/ML
General Hospital
174d
Cleared
Jan 28, 2010
MEDEFIL'S NORMAL SALINE I.V. FLUSH SYRINGE
General Hospital
240d
Cleared
Jun 24, 2002
MEDEFIL'S HEPARIN I.V. FLUSH SYRINGE IN VARIOUS FILL SIZES - 1 ML FILL IN 6...
General Hospital
88d
Cleared
Jun 20, 2002
MEDEFIL'S NORMAL SALINE FLUSH SYRINGE IN VARIOUS FILL SIZES - 1 ML FILL IN 6...
General Hospital
84d
Cleared
Jun 12, 2000
MEDEFIL'S HEPARIN I.V. FLUSH SYRINGE, IN VARIOUS FILL SIZES - 1 ML FILL IN 3...
General Hospital
238d
Cleared
Feb 25, 2000
MEDEFIL'S NORMAL SALINE FLUSH SYRINGE, IN VARIOUS FILL SIZES - 1 ML FILL IN 3...
General Hospital
130d