510(k) K232442

Device
Disposable Endoscope Injection Needles
Applicant
Zhejiang Soudon Medical Technology Co., Ltd.
510(k) number
K232442
Product code
FBK
Decision
Substantially Equivalent (SESE)
Decision date
2023-11-09
Date received
2023-08-14
Regulation
876.1500
Classification name
Endoscopic Injection Needle, Gastroenterology-Urology
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Junshi Wang
Address
Rm. 302-1, Floor 3, Bldg. 4, #1 Nangonghe Rd., Donghu St., Linping District Hangzhou CN 311100 311100

FDA Registration Numbers

Source Documents

510(k) summary PDF

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