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MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM

Page Type
Cleared 510(K)
510(k) Number
K864837
510(k) Type
Traditional
Applicant
OEC-DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1987
Days to Decision
52 days

MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM

Page Type
Cleared 510(K)
510(k) Number
K864837
510(k) Type
Traditional
Applicant
OEC-DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1987
Days to Decision
52 days