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Nicolet Instrument Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K921138NICOLET ULTRASOM ACQUISITION STATIONMay 14, 1993
K923315NICOLET ARK SYSTEMNovember 23, 1992
K921927NICOLET VOYAGEURNovember 5, 1992
K915652NICOLET PORATBLE SPIRIT SYSTEMFebruary 7, 1992
K905632NICOLET MAPLELEAF SYSTEMJune 7, 1991
K897154NICOLET DBTE HEARING AID: DIGITAL & PROGRAMMABLEApril 30, 1990
K894629NICOLET BEAM II SYSTEMMarch 9, 1990
K896477NICOLET REAL EAR ANALYZERFebruary 8, 1990
K883781NICOLET NEUROPORT/ACE SYSTEMJune 5, 1989
K890495NICOLET VIKING II SYSTEMMarch 16, 1989
K884294NICOLET NYSTAR PLUS SYSTEMNovember 23, 1988
K882599NICOLET BRAINLAB SYSTEMOctober 19, 1988
K882053NICOLET EPIDURAL SPINAL ELECTRODEOctober 18, 1988