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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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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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