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FDA 510(k) K133338, LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX), by Covidien, Formerly Valleylab, A Division of Tyco H
FDA 510(k) K133338, LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX), by Covidien, Formerly Valleylab, A Division of Tyco H
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510(K) Number: K133338
Device Name: LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX)
Manufacturer: Covidien, Formerly Valleylab, A Division of Tyco H
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/30/2013
Decision Date: 12/20/2013
Regulation Medical Specialty: General & Plastic Surgery
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