510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K841403Substantially Equivalent

Hemo-Ro Water Purification Sys

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

K841403 is the FDA 510(k) clearance record for HEMO-RO WATER PURIFICATION SYS, a class II device, cleared for Millipore Corp. on under FDA product code FIP (Subsystem, Water Purification). FDA records list 94 510(k) clearances for EMD MILLIPORE CORPORATION, from to . As of , FDA records show no recalls naming K841403.

Clearance record

Decision date
Received
(94 days to decision)
Product code
FIP Subsystem, Water Purification
Regulation
21 CFR 876.5665
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Millipore Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FIP

Trailing 12 months
1 clearance under product code FIP in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FIP, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260