510(k) K222006

Device
Sclerotherapy & Endoscopic Needles
Applicant
G-Flex Europe Sprl
510(k) number
K222006
Product code
FBK
Decision
Substantially Equivalent (SESE)
Decision date
2023-04-03
Date received
2022-07-07
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
Thierry Cremer
Address
20, Rue De LÂ’Industrie Nivelles BE 1400 1400

FDA Registration Numbers

Source Documents

510(k) summary PDF

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