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FDA 510(k), K093358, MICROPLEX COIL SYSTEM-COSMOS, MODELS 81451CS-V, 181555CS-V, 16=81652CS-V
FDA 510(k), K093358, MICROPLEX COIL SYSTEM-COSMOS, MODELS 81451CS-V, 181555CS-V, 16=81652CS-V
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510(K) Number: K093358
Device Name: MICROPLEX COIL SYSTEM-COSMOS, MODELS 81451CS-V, 181555CS-V, 16=81652CS-V
Manufacturer: MICROVENTION, INC.
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/28/2009
Decision Date: 01/15/2010
Regulation Medical Specialty: Neurology
Device Name: MICROPLEX COIL SYSTEM-COSMOS, MODELS 81451CS-V, 181555CS-V, 16=81652CS-V
Manufacturer: MICROVENTION, INC.
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/28/2009
Decision Date: 01/15/2010
Regulation Medical Specialty: Neurology
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