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MODIFICATION TO SCINTRON IV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101013
510(k) Type
Special
Applicant
Miegmbh
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2010
Days to Decision
56 days
Submission Type
Summary

MODIFICATION TO SCINTRON IV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101013
510(k) Type
Special
Applicant
Miegmbh
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2010
Days to Decision
56 days
Submission Type
Summary