Last synced on 25 April 2025 at 11:05 pm

MYLAB 90 ULTRASOUND IMAGING SYSTEM, MODEL 6100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051837
510(k) Type
Traditional
Applicant
ESAOTE, S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2005
Days to Decision
14 days
Submission Type
Summary

MYLAB 90 ULTRASOUND IMAGING SYSTEM, MODEL 6100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051837
510(k) Type
Traditional
Applicant
ESAOTE, S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2005
Days to Decision
14 days
Submission Type
Summary