FDA 510(k), K841695, CRAWLER

FDA 510(k), K841695, CRAWLER

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510(K) Number: K841695
Device Name: CRAWLER
Manufacturer: MADDAK, INC.
Device Classification Name: Board, Scooter, Prone
Regulation Number: 890.5370
Classification Product Code: KNL
Date Received: 04/23/1984
Decision Date: 05/10/1984
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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