FDA 510(k) K002138, PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380, by Maersk Medical A/S
FDA 510(k) K002138, PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380, by Maersk Medical A/S
Device Name: PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
Manufacturer: Maersk Medical A/S
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 07/17/2000
Decision Date: 08/29/2000
Regulation Medical Specialty: General Hospital
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