510(k) K241523

Device
injeTAK Adjustable Tip Needle (DIS199; DIS201)
Applicant
Laborie Medical Technologies, Corp.
510(k) number
K241523
Product code
FBK
Decision
Substantially Equivalent (SESE)
Decision date
2024-08-27
Date received
2024-05-29
Regulation
876.1500
Classification name
Endoscopic Injection Needle, Gastroenterology-Urology
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Thomas Hirte
Address
180 International Dr. Portsmouth NH US 03801 03801

FDA Registration Numbers

Source Documents

510(k) summary PDF

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