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FDA 510(k), K071934, MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT
FDA 510(k), K071934, MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT
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510(K) Number: K071934
Device Name: MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT
Manufacturer: BIOMET MANUFACTURING CORP.
Device Classification Name: Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
Regulation Number: 862.2050
Classification Product Code: JQC
Date Received: 07/13/2007
Decision Date: 10/11/2007
Regulation Medical Specialty: Clinical Chemistry
Device Name: MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT
Manufacturer: BIOMET MANUFACTURING CORP.
Device Classification Name: Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
Regulation Number: 862.2050
Classification Product Code: JQC
Date Received: 07/13/2007
Decision Date: 10/11/2007
Regulation Medical Specialty: Clinical Chemistry
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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