FDA 510(k), K002138, PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
FDA 510(k), K002138, PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
Device Name: PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
Manufacturer:
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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