FDA 510(k), K161804, LigaSure Retractable L-Hook Laparoscopic Sealer/Divider

FDA 510(k), K161804, LigaSure Retractable L-Hook Laparoscopic Sealer/Divider

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510(K) Number: K161804
Device Name: LigaSure Retractable L-Hook Laparoscopic Sealer/Divider
Manufacturer: DAWN D. TINDALL
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 06/30/2016
Date Received: 09/16/2016
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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