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MYLAB15/20 NEW INDICATIONS ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061755
510(k) Type
Traditional
Applicant
ESAOTE EUROPE B.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2006
Days to Decision
47 days
Submission Type
Summary

MYLAB15/20 NEW INDICATIONS ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061755
510(k) Type
Traditional
Applicant
ESAOTE EUROPE B.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2006
Days to Decision
47 days
Submission Type
Summary