FDA 510(k), K141119, CAMERA ENABLED PROBE

FDA 510(k), K141119, CAMERA ENABLED PROBE

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510(K) Number: K141119
Device Name: CAMERA ENABLED PROBE
Manufacturer: TRICE MEDICAL, INC.
Device Classification Name: arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/30/2014
Decision Date: 07/29/2014
Regulation Medical Specialty: Orthopedic

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