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VISTA - MODELS V12, V20, V23, V38, ITE HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902179
510(k) Type
Traditional
Applicant
VISTA LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1990
Days to Decision
87 days