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MESI mTABLET TBI diagnostic system, MESI mTABLET TBI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213730
510(k) Type
Traditional
Applicant
Mesi, Development of Medical Devices, Ltd.; Mesi d.o.o.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
4/21/2022
Days to Decision
146 days
Submission Type
Summary

MESI mTABLET TBI diagnostic system, MESI mTABLET TBI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213730
510(k) Type
Traditional
Applicant
Mesi, Development of Medical Devices, Ltd.; Mesi d.o.o.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
4/21/2022
Days to Decision
146 days
Submission Type
Summary