FDA 510(k), K964397, THERAPIK

FDA 510(k), K964397, THERAPIK

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510(K) Number: K964397
Device Name: THERAPIK
Manufacturer: THE JENEX CORPORATION
Device Classification Name: lamp, infrared, therapeutic heating
Regulation Number: 890.5500
Classification Product Code: ILY
Date Received: 11/04/1996
Decision Date: 11/04/1997
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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