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FDA 510(k), K130847, JINTRONIX REHABILITATION SYSTEM (JRS)
FDA 510(k), K130847, JINTRONIX REHABILITATION SYSTEM (JRS)
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510(K) Number: K130847
Device Name: JINTRONIX REHABILITATION SYSTEM (JRS)
Manufacturer: JINTRONIX INC.
Device Classification Name: interactive rehabilitation exercise devices
Regulation Number: 890.5360
Classification Product Code: LXJ
Date Received: 03/26/2013
Decision Date: 02/28/2014
Regulation Medical Specialty: Physical Medicine
Device Name: JINTRONIX REHABILITATION SYSTEM (JRS)
Manufacturer: JINTRONIX INC.
Device Classification Name: interactive rehabilitation exercise devices
Regulation Number: 890.5360
Classification Product Code: LXJ
Date Received: 03/26/2013
Decision Date: 02/28/2014
Regulation Medical Specialty: Physical Medicine
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- 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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