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AUDIFON H24 AGC/AUDIFON H25 AGC/AUDIFON H30 AGC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972550
510(k) Type
Traditional
Applicant
TRUTONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1997
Days to Decision
31 days
Submission Type
Statement