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Metron U.S., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K982020METRON QA-IDS I.V. PUMP TESTERSeptember 30, 1998
K973991METRON QA-510 SPO2 ANALYZERJanuary 16, 1998
K963190QA-40M DEFIBRILLATOR TESTERJuly 1, 1997
K963198PS-41 6M PATIENT SIMULATORMarch 5, 1997