Medical Device Manufacturer · US , Saint Louis , MO

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

1 submissions · 1 cleared · Since 2018

Recent clearances: BacterioScan 216Dx System

1
Total
1
Cleared
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Denied

Bacterioscan, Inc. has 1 FDA 510(k) cleared medical devices. Based in Saint Louis, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Bacterioscan, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by MDC Associates, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Bacterioscan, Inc.

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