FDA 510(k), K140560, ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING
FDA 510(k), K140560, ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING
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510(K) Number: K140560
Device Name: ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING
Manufacturer: ETHICON ENDO-SURGERY, LLC
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 03/05/2014
Decision Date: 04/22/2014
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING
Manufacturer: ETHICON ENDO-SURGERY, LLC
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 03/05/2014
Decision Date: 04/22/2014
Regulation Medical Specialty: General & Plastic Surgery
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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