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AI5200 DIAGNOSTIC ULTRASOUND SYSTEM TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895071
510(k) Type
Traditional
Applicant
ACOUSTIC IMAGING
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1989
Days to Decision
62 days

AI5200 DIAGNOSTIC ULTRASOUND SYSTEM TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895071
510(k) Type
Traditional
Applicant
ACOUSTIC IMAGING
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1989
Days to Decision
62 days