510(k) K230909

Device
EchoTip® AcuCore™ Ultrasound Biopsy Needle (ECHO-BX-3-22)
Applicant
Cook Ireland, Ltd.
510(k) number
K230909
Product code
FCG
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-30
Date received
2023-03-31
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
Laura O'Reilly
Address
O' Halloran Rd., National Technology Park, Plassey Limerick IE V94 N8X2 V94 N8X2

FDA Registration Numbers

Source Documents

510(k) summary PDF

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