510(k) K243607

Device
Moda-flx Hemodialysis System? Cartridge (102121-001 )
Applicant
Diality, Inc.
510(k) number
K243607
Product code
FJK
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-20
Date received
2024-11-21
Regulation
876.5820
Classification name
Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
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
Clayton Poppe
Address
181 Technology Dr., Suite 150 Irvine CA US 92618 92618

FDA Registration Numbers

Source Documents

510(k) summary PDF

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