Medical Device Manufacturer · US , Madison , WI

Nicolet Instrument Corp. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1988

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - Nicolet Instrument Corp. Neurology ✕

11 devices

1-11 of 11

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 Mar 09, 1990

NICOLET BEAM II SYSTEM

Neurology · 228d

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

Cleared Oct 18, 1988

NICOLET EPIDURAL SPINAL ELECTRODE

Neurology · 155d