FDA 510(k) Application Details - K232950

Device Classification Name Syringe, Piston

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510(K) Number K232950
Device Name Syringe, Piston
Applicant Perfect Medical Industry (VN) Co., Ltd.
Block D/7I, No. 1B Road, Vinh Loc Industrial Zone
Binh Hung Hoa B Ward, Bin Tan District
Ho Chi Minh City 700000 VN
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Contact Nancy Phan
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Regulation Number 880.5860

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Classification Product Code FMF
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Date Received 09/20/2023
Decision Date 06/12/2024
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

FDA Source Information for K232950


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