Home / Companies / U.S Army Medical Materiel Development Activity

U.S Army Medical Materiel Development Activity

FDA Regulatory Profile

U.S Army Medical Materiel Development Activity 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 October 1, 2015.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K152523JBAIDS Influenza A & B Detection KitOctober 1, 2015
K111778JBAIDS INFLUENZA A SUBTYPING KITSeptember 13, 2011

FDA data resources