Medical Device Manufacturer · US , Madison , WI

Nicolet Biomedical, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1995

Total

Cleared

Denied

Nicolet Biomedical, Inc. has 10 FDA 510(k) cleared neurology devices. Based in Madison, US.

Historical record: 10 cleared submissions from 1995 to 2002.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Nicolet Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nicolet Biomedical, Inc.

10 devices

1-10 of 10

SUBDURAL STRIP ELECTRODE

NICOLET ELECTROCAUTERY DETECTOR

K020955 · ETN

Ear, Nose, Throat · 23d

Cleared Sep 06, 2001

STERILE EMG ELECTRODES

STERILE SUBDERMAL NEEDLE ELECTRODES

K010019 · GXZ

Neurology · 76d

Cleared Nov 03, 1999

BRAVO MULTI-MODALITY SYSTEM

Nicolet Biomedical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Nicolet Biomedical, Inc.

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