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Midi, Inc.

FDA Regulatory Profile

Midi, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 17, 2006.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K052485SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEFJanuary 17, 2006
K020689SHERLOCK MYCOBACTERIA IDENTIFICATION SYSTEMOctober 31, 2002

FDA data resources