Nicolet Instrument Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nicolet Instrument Corp. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Nicolet Instrument Corp. has 13 FDA 510(k) cleared neurology devices. Based in Madison, US.
Historical record: 13 cleared submissions from 1988 to 1993.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nicolet Instrument Corp.
13 devices
Cleared
May 14, 1993
NICOLET ULTRASOM ACQUISITION STATION
Neurology
430d
Cleared
Nov 23, 1992
NICOLET ARK SYSTEM
Neurology
139d
Cleared
Nov 05, 1992
NICOLET VOYAGEUR
Neurology
195d
Cleared
Feb 07, 1992
NICOLET PORATBLE SPIRIT SYSTEM
Neurology
51d
Cleared
Jun 07, 1991
NICOLET MAPLELEAF SYSTEM
Neurology
172d
Cleared
Apr 30, 1990
NICOLET DBTE HEARING AID: DIGITAL & PROGRAMMABLE
Ear, Nose, Throat
125d
Cleared
Mar 09, 1990
NICOLET BEAM II SYSTEM
Neurology
228d
Cleared
Feb 08, 1990
NICOLET REAL EAR ANALYZER
Ear, Nose, Throat
87d
Cleared
Jun 05, 1989
NICOLET NEUROPORT/ACE SYSTEM
Neurology
272d
Cleared
Mar 16, 1989
NICOLET VIKING II SYSTEM
Neurology
43d
Cleared
Nov 23, 1988
NICOLET NYSTAR PLUS SYSTEM
Neurology
42d
Cleared
Oct 19, 1988
NICOLET BRAINLAB SYSTEM
Neurology
117d