Cleared Traditional

K892212 - INNOFLUOR(TM) QUINDINE CALIBATOR SET

K892212 is the FDA 510(k) clearance for INNOFLUOR(TM) QUINDINE CALIBATOR SET by Innotron of Oregon, Inc.. It is a Class 2 Toxicology device (product code DLJ) cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K892212 · Innotron of Oregon, Inc. · Toxicology device
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Jun 1989
Decision
67d
Days
Class 2
Risk

K892212 is an FDA 510(k) clearance for the INNOFLUOR(TM) QUINDINE CALIBATOR SET. Classified as Calibrators, Drug Specific (product code DLJ), Class II - Special Controls.

Submitted by Innotron of Oregon, Inc. (Portland, US). The FDA issued a Cleared decision on June 9, 1989 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3200 - 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 Innotron of Oregon, Inc. devices

Submission Details

510(k) Number K892212 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 1989
Decision Date June 09, 1989
Days to Decision 67 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 87d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DLJ Calibrators, Drug Specific
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3200
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 - DLJ Calibrators, Drug Specific

All 94
Devices cleared under the same product code (DLJ) and FDA review panel - the closest regulatory comparables to K892212.
DUPONT SALICYLATE CALIBRATOR
K904307 · E.I. Dupont DE Nemours & Co., Inc. · Nov 1990
DUPONT DRUG CLIBRATOR-B
K904303 · E.I. Dupont DE Nemours & Co., Inc. · Oct 1990
DUPONT ALCOHOL CALIBRATOR
K904308 · E.I. Dupont DE Nemours & Co., Inc. · Oct 1990
ACA VANCOMYCIN CALIBRATOR
K892901 · E.I. Dupont DE Nemours & Co., Inc. · May 1989
EMIT(R) D.A.U AMPHETAMINE CLASS LOW CALIBRATOR
K890451 · Syva Co. · Feb 1989
EMIT(R) D.A.U. AMPHETAMINE CLASS MEDIUM CALIBRATOR
K890452 · Syva Co. · Feb 1989