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FDA 510(k), K101734, VISIONSCOPE HIGH DEFINITION ENDOSCOPY CAMERA SYSTEM WITH; CAMERA CONTROL UNIT; CAMERA HANDPIECE; VISIONSCOPE ENDOSCOPES
FDA 510(k), K101734, VISIONSCOPE HIGH DEFINITION ENDOSCOPY CAMERA SYSTEM WITH; CAMERA CONTROL UNIT; CAMERA HANDPIECE; VISIONSCOPE ENDOSCOPES
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$149.00 USD
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510(K) Number: K101734
Device Name: VISIONSCOPE HIGH DEFINITION ENDOSCOPY CAMERA SYSTEM WITH; CAMERA CONTROL UNIT; CAMERA HANDPIECE; VISIONSCOPE ENDOSCOPES
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 06/21/2010
Decision Date: 09/08/2010
Regulation Medical Specialty: Orthopedic
Device Name: VISIONSCOPE HIGH DEFINITION ENDOSCOPY CAMERA SYSTEM WITH; CAMERA CONTROL UNIT; CAMERA HANDPIECE; VISIONSCOPE ENDOSCOPES
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 06/21/2010
Decision Date: 09/08/2010
Regulation Medical Specialty: Orthopedic
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