FDA 510(k) Application Details - K760772

Device Classification Name Binder, Abdominal

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510(K) Number K760772
Device Name Binder, Abdominal
Applicant TECNOL NEW JERSEY WOUND CARE, INC.
368 FAIRVIEW AVE.
HAMMONTON, NJ US
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Regulation Number 880.5160

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Classification Product Code FSD
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Date Received 10/04/1976
Decision Date 11/03/1976
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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