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GE LOGIQ 7 ULTRASOUND BT04

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041813
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2004
Days to Decision
17 days
Submission Type
Summary

GE LOGIQ 7 ULTRASOUND BT04

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041813
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2004
Days to Decision
17 days
Submission Type
Summary