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VASOVIEW DUPLEX IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861237
510(k) Type
Traditional
Applicant
SONICAID, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/14/1986
Days to Decision
103 days

VASOVIEW DUPLEX IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861237
510(k) Type
Traditional
Applicant
SONICAID, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/14/1986
Days to Decision
103 days