510(k) K191472

Device
Biopsy Needle
Applicant
Ushare Medical, Inc.
510(k) number
K191472
Product code
FCG
Decision
Substantially Equivalent (SESE)
Decision date
2020-01-29
Date received
2019-06-03
Regulation
876.1075
Classification name
Biopsy Needle
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Yan Wang
Address
445 An Ji Zhong Rd., San Zao Town Zhuhai CN 519090 519090

FDA Registration Numbers

Source Documents

510(k) summary PDF

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