FDA 510(k) Application Details - K211509

Device Classification Name Gown, Surgical

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510(K) Number K211509
Device Name Gown, Surgical
Applicant Hubei Wanli Protective Products Co. Ltd
Tangwan Street, Xiliuhe Town
XianTao CN
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Contact Andy Wen
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Regulation Number 878.4040

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Classification Product Code FYA
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Date Received 05/14/2021
Decision Date 10/24/2021
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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