Cleared Traditional

QUANTIMETRIC PLUS LAMBDA REAGENT KIT

K855007 · Kallestad Laboratories, Inc. · Immunology
Feb 1986
Decision
72d
Days
Class 2
Risk

About This 510(k) Submission

K855007 is an FDA 510(k) clearance for the QUANTIMETRIC PLUS LAMBDA REAGENT KIT, a Lambda, Antigen, Antiserum, Control (Class II — Special Controls, product code DEH), submitted by Kallestad Laboratories, Inc. (Chaska, US). The FDA issued a Cleared decision on February 26, 1986, 72 days after receiving the submission on December 16, 1985. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5550.

Submission Details

510(k) Number K855007 FDA.gov
FDA Decision Cleared SESE
Date Received December 16, 1985
Decision Date February 26, 1986
Days to Decision 72 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary —

Device Classification

Product Code DEH — Lambda, Antigen, Antiserum, Control
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.5550

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