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MODIFICATIONS TO EUB-525 DIAGNOSTIC ULTRASOUND SCANNER; EUB-2000 DIAGNOSTIC ULTRASOUND SCANNER; SP-711 SONOPROBE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012239
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2001
Days to Decision
24 days
Submission Type
Summary

MODIFICATIONS TO EUB-525 DIAGNOSTIC ULTRASOUND SCANNER; EUB-2000 DIAGNOSTIC ULTRASOUND SCANNER; SP-711 SONOPROBE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012239
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2001
Days to Decision
24 days
Submission Type
Summary