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MIS AURAL ACOUSTIC SCREENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791170
510(k) Type
Traditional
Applicant
MAICO HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
6/25/1979
Days to Decision
0 days

MIS AURAL ACOUSTIC SCREENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791170
510(k) Type
Traditional
Applicant
MAICO HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
6/25/1979
Days to Decision
0 days