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FDA 510(k), K083707, ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE
FDA 510(k), K083707, ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE
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$149.00 USD
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Sale price
$149.00 USD
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510(K) Number: K083707
Device Name: ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/15/2008
Decision Date: 08/03/2009
Regulation Medical Specialty: Orthopedic
Device Name: ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/15/2008
Decision Date: 08/03/2009
Regulation Medical Specialty: Orthopedic
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