Cleared Traditional

K901637 - RESUBMITTED MODIFIED RUBALEX

K901637 is an FDA 510(k) clearance for RESUBMITTED MODIFIED RUBALEX, manufactured by Orion Corp.. The device is a Class 2 Microbiology device with product code LQN cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K901637 · Orion Corp. · Microbiology device
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Apr 1990
Decision
17d
Days
Class 2
Risk

K901637 is an FDA 510(k) clearance for the RESUBMITTED MODIFIED RUBALEX. Classified as Latex Agglutination Assay, Rubella (product code LQN), Class II - Special Controls.

Submitted by Orion Corp. (20101 Turku, FI). The FDA issued a Cleared decision on April 26, 1990 after a review of 17 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3510 - the FDA microbiology 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 Orion Corp. devices

FDA 510(k) Submission Details - K901637

510(k) Number K901637 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 09, 1990
Decision Date April 26, 1990
Days to Decision 17 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 102d · This submission: 17d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LQN Device Classification - Class 2, Special Controls

Product Code LQN Latex Agglutination Assay, Rubella
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3510
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 Microbiology devices follow this clearance model.

Regulatory Peers - LQN Latex Agglutination Assay, Rubella

Devices cleared under the same product code (LQN) and FDA review panel - the closest regulatory comparables to K901637.
COLORSLIDER RUBELLA
K952544 · Seradyn, Inc. · Jan 1996
RUBALEX, MODIFICATION
K912391 · Orion Corp. · May 1992
RUBALEX (REVISED VERSION)
K861881 · Orion Corp. · Jun 1986
RUBALEX
K852788 · Orion Corp. · Mar 1986
VIROGEN RUBELLA MICROTITER TEST
K844436 · Armkel, LLC · May 1985
VIROGEN RUBELLA SLIDE TEST
K844435 · Armkel, LLC · May 1985