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AP X-RAY TUBE ANGULATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K811970
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1981
Days to Decision
34 days

AP X-RAY TUBE ANGULATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K811970
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1981
Days to Decision
34 days