Cleared Traditional

K790360 - QUANTAZYME TOXOPLASMA

K790360 is an FDA 510(k) clearance for QUANTAZYME TOXOPLASMA, manufactured by Bio-Rad. The device is a Class 2 Microbiology device with product code GLZ cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K790360 · Bio-Rad · Microbiology device
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May 1979
Decision
89d
Days
Class 2
Risk

K790360 is an FDA 510(k) clearance for the QUANTAZYME TOXOPLASMA. Classified as Antigens, If, Toxoplasma Gondii (product code GLZ), Class II - Special Controls.

Submitted by Bio-Rad (Mchenry, US). The FDA issued a Cleared decision on May 22, 1979 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3780 - 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 Bio-Rad devices

FDA 510(k) Submission Details - K790360

510(k) Number K790360 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 1979
Decision Date May 22, 1979
Days to Decision 89 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
13d faster than avg
Panel avg: 102d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GLZ Device Classification - Class 2, Special Controls

Product Code GLZ Antigens, If, Toxoplasma Gondii
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3780
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 - GLZ Antigens, If, Toxoplasma Gondii

All 8
Devices cleared under the same product code (GLZ) and FDA review panel - the closest regulatory comparables to K790360.
ANTI-TOXOPLASMA GONDII KIT
K842664 · Amico Lab, Inc. · Aug 1984
TOXOPLASMA ANTIBODY TEST SYSTEM
K791571 · Zeus Scientific, Inc. · Sep 1979
FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO
K790464 · Intl. Diagnostic Technology · Jun 1979
IMMUNOZYME TOXOPLASMA ANTIBODY
K780352 · Millipore Corp. · Jun 1978
TOXO TEST
K772243 · Gull Laboratories, Inc. · Dec 1977