Last synced on 14 November 2025 at 11:06 pm

EARCHECK

Page Type
Cleared 510(K)
510(k) Number
K971859
510(k) Type
Traditional
Applicant
MDI INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
90 days
Submission Type
Summary

EARCHECK

Page Type
Cleared 510(K)
510(k) Number
K971859
510(k) Type
Traditional
Applicant
MDI INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
90 days
Submission Type
Summary