510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K925403Substantially Equivalent

Baxter Apd 12' Extension Line

Baxter Healthcare Corporation, Waukegan IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925403 is the FDA 510(k) clearance record for BAXTER APD 12' EXTENSION LINE, a class II device, cleared for Baxter Healthcare Corp on under FDA product code KDJ (Set, Administration, For Peritoneal Dialysis, Disposable). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K925403.

Clearance record

Decision date
Received
(487 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
Baxter Healthcare Corp 1500 Waukegan Rd., Waukegan IL
510(k) summary
Summary
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