FDA 510(k), K905685, ZENITH COX FLEXION CHIROPRACTIC TABLE

FDA 510(k), K905685, ZENITH COX FLEXION CHIROPRACTIC TABLE

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510(K) Number: K905685
Device Name: ZENITH COX FLEXION CHIROPRACTIC TABLE
Manufacturer: WILLIAMS MANUFACTURING CO.
Device Classification Name: table, powered
Regulation Number: 890.3760
Classification Product Code: INQ
Date Received: 12/19/1990
Decision Date: 01/18/1991
Regulation Medical Specialty: Physical Medicine
  • 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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