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MIE SCINTRON GAMMA CAMERA SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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