FDA 510(k) Application Details - K162442

Device Classification Name Gown, Surgical

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510(K) Number K162442
Device Name Gown, Surgical
Applicant GRI MEDICAL & ELECTRICAL TECHNOLOGY CO., LTD.
1805 HONGGAO ROAD, XIUZHOU INDUSTRY ZONE
JIAXING 314031 CN
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Contact Martin D. Paugh
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Regulation Number 878.4040

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Classification Product Code FYA
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Date Received 08/31/2016
Decision Date 12/12/2016
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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