Nicolet Biomedical - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Nicolet Biomedical has 8 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 8 cleared submissions from 1998 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Nicolet Biomedical Filter by specialty or product code using the sidebar.
8 devices
Cleared
Apr 21, 2003
NICOLET PIONEER TC8080
Radiology
410d
Cleared
Apr 18, 2002
VERSALAB APM
Obstetrics & Gynecology
198d
Cleared
Dec 20, 2001
NICOLET ELECTROMAGNETIC NAVIGATION SYSTEM
Radiology
66d
Cleared
Jul 26, 2001
GSI AUDERA
Ear, Nose, Throat
104d
Cleared
Mar 09, 2001
NICOLET VERSALAB
Radiology
15d
Cleared
Nov 30, 2000
NICOLET VASOGUARD
Cardiovascular
86d
Cleared
Jun 29, 2000
NICOLET EME LEGEND TC22
Radiology
223d
Cleared
Aug 07, 1998
CAREDOP II
Radiology
25d