FDA 510(k), K933768, COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES

FDA 510(k), K933768, COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES

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510(K) Number: K933768
Device Name: COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES
Manufacturer:
Device Classification Name: Laparoscope, Gynecologic (And Accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 07/29/1993
Decision Date: 06/27/1994
Regulation Medical Specialty: Obstetrics/Gynecology
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