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GYROSCAN T5 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K890789
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1989
Days to Decision
72 days

GYROSCAN T5 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K890789
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1989
Days to Decision
72 days