Cleared Traditional

K852751 - TOLVIDINE RED UNHEATED SERUM SYPHILLIS ...

K852751 is the FDA 510(k) clearance for TOLVIDINE RED UNHEATED SERUM SYPHILLIS ... by Preco, Inc.. It is a Class 2 Microbiology device (product code GMQ) cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K852751 · Preco, Inc. · Microbiology device
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Aug 1985
Decision
53d
Days
Class 2
Risk

K852751 is an FDA 510(k) clearance for the TOLVIDINE RED UNHEATED SERUM SYPHILLIS CARD TEST. Classified as Antigens, Nontreponemal, All (product code GMQ), Class II - Special Controls.

Submitted by Preco, Inc. (Oakland, US). The FDA issued a Cleared decision on August 20, 1985 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3820 - 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 Preco, Inc. devices

Submission Details

510(k) Number K852751 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 1985
Decision Date August 20, 1985
Days to Decision 53 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 102d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GMQ Antigens, Nontreponemal, All
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3820
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 - GMQ Antigens, Nontreponemal, All

All 14
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