Medical Device Manufacturer · US , Madison , WI

Promega Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021

Official Website

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Promega Corporation Pathology ✕

1 devices

1-1 of 1

Cleared Jul 26, 2021

OncoMate MSI Dx Analysis System

Pathology · 552d