Cleared Traditional

K894852 - SERACHEM PLUS CLINICAL CHEMISTRY CONTROLS

K894852 is the FDA 510(k) clearance for SERACHEM PLUS CLINICAL CHEMISTRY CONTROLS by Instrumentation Laboratory CO. It is a Class 1 Chemistry device (product code JJY) cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K894852 · Instrumentation Laboratory CO · Chemistry device
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Sep 1989
Decision
59d
Days
Class 1
Risk

K894852 is an FDA 510(k) clearance for the SERACHEM PLUS CLINICAL CHEMISTRY CONTROLS. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Instrumentation Laboratory CO (Lexington, US). The FDA issued a Cleared decision on September 28, 1989 after a review of 59 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Instrumentation Laboratory CO devices

Submission Details

510(k) Number K894852 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 31, 1989
Decision Date September 28, 1989
Days to Decision 59 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 88d · This submission: 59d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJY Multi-analyte Controls, All Kinds (assayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JJY Multi-analyte Controls, All Kinds (assayed)

All 322
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K894852.
DADE(R) TDM CONTROL
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NORMAL AND ABNORMAL CONTROL SERA
K895943 · Sclavo, Inc. · Dec 1989
LYPHOCHEK(R) TUMOR MARKER CONTROLS, LEVELS I & II
K894078 · Bio-Rad · Aug 1989
LYPHOCHEK IMMUNOASSAY PLUS CONTROL SERUM
K894252 · Bio-Rad · Aug 1989
DADE LIPID-TROL
K893580 · Baxter Healthcare Corp · Jul 1989