510(k) K222318

Device
Fresenius Liberty Select Cycler
Applicant
Fresenius Medical Care Renal Therapies Group, LLC
510(k) number
K222318
Product code
FKX
Decision
Substantially Equivalent (SESE)
Decision date
2022-10-31
Date received
2022-08-02
Regulation
876.5630
Classification name
System, Peritoneal, Automatic Delivery
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Denise Oppermann
Address
920 Winter St. Waltham MA US 02451 02451

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code FKX

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K141145LIBERTY PDX CYCLERFresenius Medical Care Renal Therapies Group, LLC2014-07-30
K123630FRESENIUS LIBERTY CYCLERFresenius Medical Care North America, Design Cente2013-09-09
K124018AMIA AUTOMATED PD SYSTEMDeka Research & Development Corp.2013-06-14
K103220VOYAGER PERITONEAL DIALYSIS SYSTEMDeka Research & Development Corp.2011-07-29
K102936HOMECHOICE/HOMECHOICE PRO AUTOMATED PERSONAL CYCLER PERITONEAL DIALYSIS SYSTEM MODEL 5C4471, 5C8310, 5C4471R AND 5C8310RBaxter Healthcare Corp2011-03-30