Neometrics, Inc. is one of 4922 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neometrics, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Neometrics, Inc. has 21 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1978 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Neometrics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neometrics, Inc.
21 devices
Cleared
Oct 23, 2015
Bard Snare Retrieval Kit
Cardiovascular
44d
Cleared
Mar 16, 2015
NovaGold High Performance Guidewire
Gastroenterology & Urology
42d
Cleared
Feb 20, 2015
Spring Coil Guidewire
Cardiovascular
112d
Cleared
Feb 20, 2014
NOVAGOLD HIGH PERFORMANCE GUIDEWIRE
Gastroenterology & Urology
143d
Cleared
Jan 03, 2013
NEO ERCP GUIDEWIRE
Gastroenterology & Urology
56d
Cleared
Sep 23, 2010
NEOWIRE PTA/PTCA GUIDEWIRE
Cardiovascular
94d
Cleared
Feb 15, 2007
VASCUPUNCTURE PICC GUIDEWIRE
Cardiovascular
30d
Cleared
Mar 01, 2005
MODIFICATION TO VASCUPUNCTURE PICC GUIDEWIRE
Cardiovascular
81d
Cleared
Apr 19, 2004
VASCUPUNCTURE PICC GUIDEWIRE WITH HYDRO-SILK COATING
Cardiovascular
21d
Cleared
Nov 05, 2003
SELECTIVA SB GUIDEWIRE
Cardiovascular
21d
Cleared
Sep 30, 2003
VASCUPUNCTURE PICC GUIDEWIRE
Cardiovascular
125d
Cleared
Feb 05, 2002
VASCUPUNCTURE ACCESS WIRE
Cardiovascular
165d