FDA 510(k) Application Details - K220157

Device Classification Name

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510(K) Number K220157
Device Name Disposable Hemostatic Closure Clip Device
Applicant Micro-Tech (Nanjing) Co., Ltd.
No. 10 Gaoke Third Road, Nanjing National Hi-Tech Industrial
Development Zone
Nanjing 210032 CN
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Contact Sally He
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Regulation Number

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Classification Product Code PKL
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Date Received 01/19/2022
Decision Date 06/13/2022
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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