Cleared Traditional

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM

K872582 · Millipore Corp. · Chemistry
Jul 1987
Decision
16d
Days
Class 1
Risk

About This 510(k) Submission

K872582 is an FDA 510(k) clearance for the HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM, a Instrumentation, High Pressure Liquid Chromatography (Class I — General Controls, product code LDM), submitted by Millipore Corp. (Milford, US). The FDA issued a Cleared decision on July 16, 1987, 16 days after receiving the submission on June 30, 1987. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2260.

Submission Details

510(k) Number K872582 FDA.gov
FDA Decision Cleared SESE
Date Received June 30, 1987
Decision Date July 16, 1987
Days to Decision 16 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

Product Code LDM — Instrumentation, High Pressure Liquid Chromatography
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.2260