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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, Biopsy, Electric
510(k) Number K180018
Device Name Disposable Hot Biopsy Forceps
Applicant
Micro-Tech (Nanjing) Co., Ltd.
#10 Gaoke Third Rd.
Nanjing,  CN 210032
Applicant Contact Becky Li
Correspondent
Micro-Tech (Nanjing) Co., Ltd.
#10 Gaoke Third Rd.
Nanjing,  CN 210032
Correspondent Contact Becky Li
Regulation Number876.4300
Classification Product Code
KGE  
Date Received01/02/2018
Decision Date 07/05/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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