FDA 510(k), K935538, BAUER TEMNO COAXIAL NEEDLE

FDA 510(k), K935538, BAUER TEMNO COAXIAL NEEDLE

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510(K) Number: K935538
Device Name: BAUER TEMNO COAXIAL NEEDLE
Manufacturer: PATRICK J LAMB
Device Classification Name: Guide, Needle, Surgical
Regulation Number: GDF
Classification Product Code: KXA
Date Received: 11/16/1993
Decision Date: 02/22/1994
Decision: Substantially Equivalent (SESE)
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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