510(k) K231861

Device
EndoflipTM 300 System
Applicant
Covidien, LLC
510(k) number
K231861
Product code
FFX
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-21
Date received
2023-06-23
Regulation
876.1725
Classification name
System, Gastrointestinal Motility (Electrical)
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Viviana Gonzalez
Address
3062 Bunkerhill Ln. Santa Clara CA US 95054 95054

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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