FDA 510(k), K943305, OLYMPUS 3D SURGICAL ENDOSCOPY SYSTEM

FDA 510(k), K943305, OLYMPUS 3D SURGICAL ENDOSCOPY SYSTEM

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510(K) Number: K943305
Device Name: OLYMPUS 3D SURGICAL ENDOSCOPY SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, Gynecologic (And Accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 07/08/1994
Decision Date: 11/17/1995
Regulation Medical Specialty: Obstetrics/Gynecology
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