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FDA 510(k), K003128, MODIFICATION TO RELIEF BRIEF
FDA 510(k), K003128, MODIFICATION TO RELIEF BRIEF
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510(K) Number: K003128
Device Name: MODIFICATION TO RELIEF BRIEF
Manufacturer: THE JM KOHN CO.
Device Classification Name: orthosis, truncal, for dysmenorrhea
Regulation Number: 890.3490
Classification Product Code: NJB
Date Received: 10/06/2000
Decision Date: 08/12/2002
Regulation Medical Specialty: Physical Medicine
Device Name: MODIFICATION TO RELIEF BRIEF
Manufacturer: THE JM KOHN CO.
Device Classification Name: orthosis, truncal, for dysmenorrhea
Regulation Number: 890.3490
Classification Product Code: NJB
Date Received: 10/06/2000
Decision Date: 08/12/2002
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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