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SERIES 6600 DIGITAL MOBILE C-ARM

Page Type
Cleared 510(K)
510(k) Number
K951765
510(k) Type
Traditional
Applicant
GE DEC MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1995
Days to Decision
24 days
Submission Type
Summary

SERIES 6600 DIGITAL MOBILE C-ARM

Page Type
Cleared 510(K)
510(k) Number
K951765
510(k) Type
Traditional
Applicant
GE DEC MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1995
Days to Decision
24 days
Submission Type
Summary