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ARTIS 3200 DIAGNOSTIC ULTRASOUND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K875251
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1988
Days to Decision
141 days

ARTIS 3200 DIAGNOSTIC ULTRASOUND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K875251
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1988
Days to Decision
141 days