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GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032656
510(k) Type
Special
Applicant
Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
63 days
Submission Type
Summary

GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032656
510(k) Type
Special
Applicant
Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
63 days
Submission Type
Summary