FDA 510(k), K931621, ACUFEX PRO-PAC AND ISO-PAC

FDA 510(k), K931621, ACUFEX PRO-PAC AND ISO-PAC

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510(K) Number: K931621
Device Name: ACUFEX PRO-PAC AND ISO-PAC
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/02/1993
Decision Date: 01/21/1994
Regulation Medical Specialty: Orthopedic
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