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HISPEED CT/I WITH PERFORMIX TUBE AND WARP SCAN OPTION

Page Type
Cleared 510(K)
510(k) Number
K964746
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1997
Days to Decision
59 days
Submission Type
Summary

HISPEED CT/I WITH PERFORMIX TUBE AND WARP SCAN OPTION

Page Type
Cleared 510(K)
510(k) Number
K964746
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1997
Days to Decision
59 days
Submission Type
Summary