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FDA 510(k), K903820, THERA-CANE
FDA 510(k), K903820, THERA-CANE
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510(K) Number: K903820
Device Name: THERA-CANE
Manufacturer: PRO MESSAGE CO.
Device Classification Name: massager, therapeutic, manual
Regulation Number: 890.5660
Classification Product Code: LYG
Date Received: 08/20/1990
Decision Date: 09/19/1990
Regulation Medical Specialty: Physical Medicine
Device Name: THERA-CANE
Manufacturer: PRO MESSAGE CO.
Device Classification Name: massager, therapeutic, manual
Regulation Number: 890.5660
Classification Product Code: LYG
Date Received: 08/20/1990
Decision Date: 09/19/1990
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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