510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872582Substantially Equivalent

High Pressure Liquid Chromatography System

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

K872582 is the FDA 510(k) clearance record for HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM, a class I device, cleared for Millipore Corp. on under FDA product code LDM (Instrumentation, High Pressure Liquid Chromatography). FDA records list 94 510(k) clearances for EMD MILLIPORE CORPORATION, from to . As of , FDA records show no recalls naming K872582.

Clearance record

Decision date
Received
(16 days to decision)
Product code
LDM Instrumentation, High Pressure Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Millipore Corp. 34 Maple St., Milford MA
Third party review
No

Clearances, product code LDM

Trailing 12 months

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

FDA records show no clearances under product code LDM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDM, 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