Cleared Traditional

K840193 - EMIT QST AMIKACIN ASSAY

K840193 is the FDA 510(k) clearance for EMIT QST AMIKACIN ASSAY by Syva Co.. It is a Class 2 Toxicology device (product code KLQ) cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K840193 · Syva Co. · Toxicology device
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Mar 1984
Decision
65d
Days
Class 2
Risk

K840193 is an FDA 510(k) clearance for the EMIT QST AMIKACIN ASSAY. Classified as Radioimmunoassay, Amikacin (product code KLQ), Class II - Special Controls.

Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on March 23, 1984 after a review of 65 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3035 - the FDA toxicology device 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 Syva Co. devices

Submission Details

510(k) Number K840193 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 1984
Decision Date March 23, 1984
Days to Decision 65 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 87d · This submission: 65d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KLQ Radioimmunoassay, Amikacin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3035
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 Toxicology devices follow this clearance model.

Regulatory Peers - KLQ Radioimmunoassay, Amikacin

All 11
Devices cleared under the same product code (KLQ) and FDA review panel - the closest regulatory comparables to K840193.
RANDOX AMIKACIN
K033884 · Randox Laboratories, Ltd. · Jun 2004
COBAS FP REAGEN FOR AMIKACIN & AMIKACIN CALIBRATOR
K852317 · Roche Diagnostic Systems, Inc. · Jun 1985
AMIKACIN ANALYTICAL TEST PACK ACA
K843211 · E.I. Dupont DE Nemours & Co., Inc. · Sep 1984
STRATUS AMIKACIN FLUOROMETRIC
K832336 · American Dade · Aug 1983
EMIT-AMD AMIKACIN ASSAY
K822657 · Dade Behring, Inc. · Sep 1982
MACRO-VUE CARD TEST, AMIKACIN
K821771 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jun 1982