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EARCHECK PRO

Page Type
Cleared 510(K)
510(k) Number
K970685
510(k) Type
Traditional
Applicant
MDI INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1997
Days to Decision
93 days
Submission Type
Summary

EARCHECK PRO

Page Type
Cleared 510(K)
510(k) Number
K970685
510(k) Type
Traditional
Applicant
MDI INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1997
Days to Decision
93 days
Submission Type
Summary