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FDA 510(k), K133941, MITEK ARTHROSCOPES
FDA 510(k), K133941, MITEK ARTHROSCOPES
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$149.00 USD
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$149.00 USD
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510(K) Number: K133941
Device Name: MITEK ARTHROSCOPES
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/23/2013
Decision Date: 04/18/2014
Regulation Medical Specialty: Orthopedic
Device Name: MITEK ARTHROSCOPES
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/23/2013
Decision Date: 04/18/2014
Regulation Medical Specialty: Orthopedic
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