FDA 510(k), K030009, KSEA POWERSHAVER SYSTEM S2
FDA 510(k), K030009, KSEA POWERSHAVER SYSTEM S2
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510(K) Number: K030009
Device Name: KSEA POWERSHAVER SYSTEM S2
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 01/02/2003
Decision Date: 04/02/2003
Regulation Medical Specialty: Orthopedic
Device Name: KSEA POWERSHAVER SYSTEM S2
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 01/02/2003
Decision Date: 04/02/2003
Regulation Medical Specialty: Orthopedic