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OMNITON MT80-A BODY HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800779
510(k) Type
Traditional
Applicant
BOSCH HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
57 days

OMNITON MT80-A BODY HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800779
510(k) Type
Traditional
Applicant
BOSCH HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
57 days