Medical Device Manufacturer · US , Mchenry , IL

Honeywell, Inc. - FDA 510(k) Cleared Devices

69 submissions · 69 cleared · Since 1976

69

Total

69

Cleared

0

Denied

FDA 510(k) Regulatory Record - Honeywell, Inc. Neurology ✕

2 devices

1-2 of 2

Cleared Nov 21, 1977

AMPLIFIER OTRONA, MODEL N3A-EMG

Neurology · 14d

Cleared Sep 20, 1977

AMPLIFIER MODEL N3B-EEG

Neurology · 14d