510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K803275Substantially Equivalent

Kpp Peritoneal Dialysate Filter

EMD Millipore Corporation, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K803275 is the FDA 510(k) clearance record for KPP PERITONEAL DIALYSATE FILTER, a class II device, cleared for Millipore Corp. on under FDA product code KPP (Peritoneal Dialysate Filter). FDA records list 94 510(k) clearances for EMD MILLIPORE CORPORATION, from to . As of , FDA records show no recalls naming K803275.

Clearance record

Decision date
Received
(74 days to decision)
Product code
KPP Peritoneal Dialysate Filter
Regulation
21 CFR 876.5630
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Millipore Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KPP

Trailing 12 months

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

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