Cleared Traditional

K903201 - ACCUPROBE BLASTOMYCES DERMATIT CULT CONFIRM TEST (FDA 510(k) Clearance)

Class II Microbiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K903201 · Gen-Probe, Inc. · Microbiology device
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Sep 1990
Decision
54d
Days
Class 2
Risk

K903201 is an FDA 510(k) clearance for the ACCUPROBE BLASTOMYCES DERMATIT CULT CONFIRM TEST. Classified as Dna-probe - Blastomyces Dermatitidis (product code MDC), Class II - Special Controls.

Submitted by Gen-Probe, Inc. (San Diego, US). The FDA issued a Cleared decision on September 12, 1990 after a review of 54 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3060 - 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 Gen-Probe, Inc. devices

Submission Details

510(k) Number K903201 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 1990
Decision Date September 12, 1990
Days to Decision 54 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 102d · This submission: 54d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MDC Dna-probe - Blastomyces Dermatitidis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3060
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.