510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772236Substantially Equivalent

Filter, Peritoneal Dialy. Admin. Set

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

K772236 is the FDA 510(k) clearance record for FILTER, PERITONEAL DIALY. ADMIN. SET, a class II device, cleared for Millipore Corp. on under FDA product code KDJ (Set, Administration, For Peritoneal Dialysis, Disposable). FDA records list 94 510(k) clearances for EMD MILLIPORE CORPORATION, from to . As of , FDA records show no recalls naming K772236.

Clearance record

Decision date
Received
(48 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
Millipore Corp. 803 N. Front St. Suite 3, Mchenry IL
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 October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KDJ, 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