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ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071287
510(k) Type
Traditional
Applicant
SHIMADZU MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2008
Days to Decision
246 days
Submission Type
Summary

ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071287
510(k) Type
Traditional
Applicant
SHIMADZU MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2008
Days to Decision
246 days
Submission Type
Summary