Medical Device Manufacturer · US , Mchenry , IL

Bendix Instruments & Life Support Div - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1978

Total

Cleared

Denied

Bendix Instruments & Life Support Div has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 1 cleared submissions from 1978 to 1978. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Bendix Instruments & Life Support Div Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bendix Instruments & Life Support Div

1 devices

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