Cleared Traditional

MODEL 250 LIQUID CHROMOTAGRAPHY PUMP

K884886 · The Perkin-Elmer Corp. · Chemistry
Feb 1989
Decision
72d
Days
Class 1
Risk

About This 510(k) Submission

K884886 is an FDA 510(k) clearance for the MODEL 250 LIQUID CHROMOTAGRAPHY PUMP, a Instrumentation, High Pressure Liquid Chromatography (Class I — General Controls, product code LDM), submitted by The Perkin-Elmer Corp. (Norwalk, US). The FDA issued a Cleared decision on February 2, 1989, 72 days after receiving the submission on November 22, 1988. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2260.

Submission Details

510(k) Number K884886 FDA.gov
FDA Decision Cleared SESE
Date Received November 22, 1988
Decision Date February 02, 1989
Days to Decision 72 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