FDA 510(k), K152618, PANTHER Cutter Stapler

FDA 510(k), K152618, PANTHER Cutter Stapler

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510(K) Number: K152618
Device Name: PANTHER Cutter Stapler
Manufacturer: B. J. ZH. F. PANTHER MEDICAL EQUIPMENT CO.,LTD
Device Classification Name: Staple, Implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 09/14/2015
Decision Date: 11/12/2015
Regulation Medical Specialty: General & Plastic Surgery
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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