FDA 510(k) Application Details - K013244

Device Classification Name Bandage, Elastic

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510(K) Number K013244
Device Name Bandage, Elastic
Applicant MED GEN, INC.
7284 W. PALMETTO PK. RD.
BOCA RATON, FL 33433-3406 US
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Contact THEDORE BARASH
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Regulation Number 880.5075

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Classification Product Code FQM
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Date Received 09/28/2001
Decision Date 12/07/2001
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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