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WIDEX MODEL SENSO DIGITAL (C8)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955878
510(k) Type
Traditional
Applicant
Widex Hearing Aid Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1996
Days to Decision
46 days
Submission Type
Statement

WIDEX MODEL SENSO DIGITAL (C8)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955878
510(k) Type
Traditional
Applicant
Widex Hearing Aid Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1996
Days to Decision
46 days
Submission Type
Statement