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LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960527
510(k) Type
Traditional
Applicant
GE Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1997
Days to Decision
580 days
Submission Type
Summary

LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960527
510(k) Type
Traditional
Applicant
GE Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1997
Days to Decision
580 days
Submission Type
Summary