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AUDIFON H20 PC/AUDIFON H32 PP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972552
510(k) Type
Traditional
Applicant
TRUTONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
30 days
Submission Type
Statement