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VIVOSONIC

Page Type
Cleared 510(K)
510(k) Number
K984562
510(k) Type
Traditional
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1999
Days to Decision
167 days
Submission Type
Statement

VIVOSONIC

Page Type
Cleared 510(K)
510(k) Number
K984562
510(k) Type
Traditional
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1999
Days to Decision
167 days
Submission Type
Statement