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DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112022
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2011
Days to Decision
69 days
Submission Type
Summary

DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112022
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2011
Days to Decision
69 days
Submission Type
Summary