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PHILIPS M30 IN-THE-EAR HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912339
510(k) Type
Traditional
Applicant
PHILIPS HEARING INSTRUMENTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1991
Days to Decision
14 days
Submission Type
Statement