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MIE SCINTRON GAMMA CAMERA SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K101768
510(k) Type
Traditional
Applicant
MIE GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
104 days
Submission Type
Summary

MIE SCINTRON GAMMA CAMERA SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K101768
510(k) Type
Traditional
Applicant
MIE GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
104 days
Submission Type
Summary