Medical Device Manufacturer · US , Newark , DE

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

2 submissions · 2 cleared · Since 2002
2
Total
2
Cleared
0
Denied

Midi, Inc. has 2 FDA 510(k) cleared medical devices. Based in Newark, US.

Historical record: 2 cleared submissions from 2002 to 2006. Primary specialty: Microbiology.

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

FDA 510(k) Regulatory Record - Midi, Inc.
2 devices
1-2 of 2
Cleared Jan 17, 2006
SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF
K052485 · NWZ
Microbiology · 130d
Cleared Oct 31, 2002
SHERLOCK MYCOBACTERIA IDENTIFICATION SYSTEM
K020689 · NJO
Microbiology · 241d
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