510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K041792Substantially Equivalent

Fresenius Staysafe Patient Connectors, Model 050-87211

Fresenius Medical Care Renal Therapies Group, LLC, Lexington MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K041792 is the FDA 510(k) clearance record for FRESENIUS STAYSAFE PATIENT CONNECTORS, MODEL 050-87211, a class II device, cleared for Fresenius Medical Care North America on under FDA product code KDJ (Set, Administration, For Peritoneal Dialysis, Disposable). FDA records list 95 510(k) clearances for Fresenius Medical Care Renal Therapies Group, LLC, from to . As of , FDA records show no recalls naming K041792.

Clearance record

Decision date
Received
(84 days to decision)
Product code
KDJ Set, Administration, For Peritoneal Dialysis, Disposable
Regulation
21 CFR 876.5630
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Fresenius Medical Care North America 95 Hayden Ave., Lexington MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KDJ

Trailing 12 months

FDA records hold no clearances under product code KDJ in the trailing twelve months.

FDA records show no clearances under product code KDJ in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KDJ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260