U.S. Safety Syringes Co., Inc. is one of 21830 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U.S. Safety Syringes Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: NOVA SAFE SCALP VEIN BLOOD COLLECTION SET, NUOVOGUARD, NUOVOCATH
7
Total
7
Cleared
0
Denied
U.S. Safety Syringes Co., Inc. has 7 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Historical record: 7 cleared submissions from 2000 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by U.S. Safety Syringes Co., Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - U.S. Safety Syringes Co., Inc.
7 devices
Cleared
Mar 10, 2009
NOVA SAFE SCALP VEIN BLOOD COLLECTION SET
General Hospital
13d
Cleared
Feb 05, 2009
NUOVOGUARD
General Hospital
15d
Cleared
Dec 04, 2008
NUOVOCATH
General Hospital
13d
Cleared
May 13, 2008
IV ADMINISTRATION SET
General Hospital
64d
Cleared
May 13, 2008
NOVOLET
General Hospital
64d
Cleared
Apr 23, 2001
SHIELDING NEEDLE HOLDER
General Hospital
174d
Cleared
Mar 08, 2000
SUPERGUARD SAFETY SYRINGE
General Hospital
362d