Cleared Traditional

K914909 - IL TEST(TM) CALIBRATION SET SP

K914909 is the FDA 510(k) clearance for IL TEST(TM) CALIBRATION SET SP by Instrumentation Laboratory CO. It is a Class 2 Chemistry device (product code JIX) cleared through the Traditional 510(k) pathway after a 82-day FDA review.

K914909 · Instrumentation Laboratory CO · Chemistry device
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Optimized for regulatory review, auditing and printing
Jan 1992
Decision
82d
Days
Class 2
Risk

K914909 is an FDA 510(k) clearance for the IL TEST(TM) CALIBRATION SET SP. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.

Submitted by Instrumentation Laboratory CO (Lexington, US). The FDA issued a Cleared decision on January 22, 1992 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 K914909 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 01, 1991
Decision Date January 22, 1992
Days to Decision 82 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
6d faster than avg
Panel avg: 88d · This submission: 82d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIX Calibrator, Multi-analyte Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JIX Calibrator, Multi-analyte Mixture

All 153
Devices cleared under the same product code (JIX) and FDA review panel - the closest regulatory comparables to K914909.
SYSTEMATE PLUS CALIBRATOR
K925101 · Em Diagnostic Systems, Inc. · Feb 1993
ROCHE CALIBRATOR SERUM
K922043 · Roche Diagnostic Systems, Inc. · Jun 1992
CIBA CORNING ACS FOLATE IMMUNOASSAY
K921678 · Ciba Corning Diagnostics Corp. · Jun 1992
DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR
K914917 · E.I. Dupont DE Nemours & Co., Inc. · Dec 1991
ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR
K914750 · Roche Diagnostic Systems, Inc. · Nov 1991
PARAMAX(R) ELECTROLYTE CALIBRATOR 1&2/MODIFICATION
K910309 · Baxter Healthcare Corp · Mar 1991