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ACCULITE(TM) OTOPROBE

Page Type
Cleared 510(K)
510(k) Number
K930981
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1993
Days to Decision
153 days
Submission Type
Summary

ACCULITE(TM) OTOPROBE

Page Type
Cleared 510(K)
510(k) Number
K930981
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1993
Days to Decision
153 days
Submission Type
Summary