Cleared Traditional

K892208 - INNOFLUOR(TM) QUINIDINE REAGENT SET

K892208 is an FDA 510(k) clearance for INNOFLUOR(TM) QUINIDINE REAGENT SET, manufactured by Innotron of Oregon, Inc.. The device is a Class 2 Toxicology device with product code LBZ cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K892208 · Innotron of Oregon, Inc. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1989
Decision
67d
Days
Class 2
Risk

K892208 is an FDA 510(k) clearance for the INNOFLUOR(TM) QUINIDINE REAGENT SET. Classified as Enzyme Immunoassay, Quinidine (product code LBZ), 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 862.3320 - 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

FDA 510(k) Submission Details - K892208

510(k) Number K892208 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
Combination Product No
PCCP Authorized No
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.

LBZ Device Classification - Class 2, Special Controls

Product Code LBZ Enzyme Immunoassay, Quinidine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3320
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 - LBZ Enzyme Immunoassay, Quinidine

All 26
Devices cleared under the same product code (LBZ) and FDA review panel - the closest regulatory comparables to K892208.
EMIT 2000 QUINDINE ASSAY QUIDIDINE CALIBRATORS
K922913 · Syva Co. · Aug 1992
EMIT CONVENIENCE PACK, QUINIDINE ASSAY/CALIBRATORS
K904990 · Syva Co. · Feb 1991
MODIFIED ACCUFLUOR QUINIDINE REAGENT & CALIBRATOR
K900705 · Innotron of Oregon, Inc. · Apr 1990
TDXR FLECAINIDE
K872175 · Abbott Laboratories · Aug 1987
EASY-TEST QUINIDINE ITEM NO. 67---/95
K864607 · Em Diagnostic Systems, Inc. · Jan 1987
EMIT QUINIDINE ASSAY
K862214 · Syva Co. · Jun 1986