FDA 510(k), K060298, PILL PHONE

FDA 510(k), K060298, PILL PHONE

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510(K) Number: K060298
Device Name: PILL PHONE
Manufacturer: VOCEL
Device Classification Name: reminder, medication
Regulation Number: 890.5050
Classification Product Code: NXQ
Date Received: 02/06/2006
Decision Date: 03/29/2006
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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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