Cleared Traditional

K923320 - QUANTA LITE ACA SCREEN

K923320 is an FDA 510(k) clearance for QUANTA LITE ACA SCREEN, manufactured by Inova Diagnostics, Inc.. The device is a Class 2 Immunology device with product code MID cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K923320 · Inova Diagnostics, Inc. · Immunology device
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Sep 1992
Decision
83d
Days
Class 2
Risk

K923320 is an FDA 510(k) clearance for the QUANTA LITE ACA SCREEN. Classified as System, Test, Anticardiolipin Immunological (product code MID), Class II - Special Controls.

Submitted by Inova Diagnostics, Inc. (San Diego, US). The FDA issued a Cleared decision on September 28, 1992 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5660 - the FDA immunology 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 Inova Diagnostics, Inc. devices

FDA 510(k) Submission Details - K923320

510(k) Number K923320 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 07, 1992
Decision Date September 28, 1992
Days to Decision 83 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement
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: 105d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MID Device Classification - Class 2, Special Controls

Product Code MID System, Test, Anticardiolipin Immunological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5660
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 Immunology devices follow this clearance model.

Regulatory Peers - MID System, Test, Anticardiolipin Immunological

All 76
Devices cleared under the same product code (MID) and FDA review panel - the closest regulatory comparables to K923320.
ANTI-CARDIOLIPIN ANTIBODY SCREENING TEST SYSTEM
K932225 · Immuno Concepts, Inc. · Jul 1993
SYNELISA CARDIOLIPIN ANTIBODIES
K924421 · Elias U.S.A., Inc. · Nov 1992
QUANTA LITE(TM) IGA ACA
K922351 · Inova Diagnostics, Inc. · Sep 1992
DIASTAT TOTAL ANTI-CARDIOLIPIN KIT
K923886 · Shield Diagnostics, Ltd. · Sep 1992
IMMUNOWELL CARDIOLIPIN ANTIBODY (IGG) TEST
K920400 · General Biometrics, Inc. · Aug 1992
IMMUNOWELL CARDIOLIPIN ANTIBODY (IGM) TEST
K920401 · General Biometrics, Inc. · Aug 1992