FDA 510(k) Application Details - K023266

Device Classification Name Gown, Surgical

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510(K) Number K023266
Device Name Gown, Surgical
Applicant PRIMELINE MEDICAL PRODUCTS, INC.
1591 FOUR ROD RD.
ALDEN, NY 14004 US
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Contact DAVID POWER
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Regulation Number 878.4040

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Classification Product Code FYA
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Date Received 09/30/2002
Decision Date 11/08/2002
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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