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Miegmbh

FDA Regulatory Profile

Miegmbh has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 27, 2020

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K201807ANCORISAug 27, 2020
K130269ECAT SCINTRON PETApr 19, 2013
K101768MIE SCINTRON GAMMA CAMERA SYSTEMSOct 5, 2010
K101013MODIFICATION TO SCINTRON IVJun 7, 2010

FDA data resources