Cleared Traditional

SERIES 10 LIQUID CHROMOTOGRAPH

K821727 · The Perkin-Elmer Corp. · Toxicology
Jun 1982
Decision
11d
Days
Class 1
Risk

About This 510(k) Submission

K821727 is an FDA 510(k) clearance for the SERIES 10 LIQUID CHROMOTOGRAPH, a Instrumentation, High Pressure Liquid Chromatography (Class I — General Controls, product code LDM), submitted by The Perkin-Elmer Corp. (Mchenry, US). The FDA issued a Cleared decision on June 22, 1982, 11 days after receiving the submission on June 11, 1982. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.2260.

Submission Details

510(k) Number K821727 FDA.gov
FDA Decision Cleared SESE
Date Received June 11, 1982
Decision Date June 22, 1982
Days to Decision 11 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary —

Device Classification

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