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GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092140
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2009
Days to Decision
37 days
Submission Type
Summary

GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092140
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2009
Days to Decision
37 days
Submission Type
Summary