Cleared Traditional

K972449 - COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL (FDA 510(k) Clearance)

Class I Microbiology device.

K972449 · Copan Italia Spa · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1997
Decision
51d
Days
Class 1
Risk

K972449 is an FDA 510(k) clearance for the COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL. Classified as Culture Media, Anaerobic Transport (product code JSL), Class I - General Controls.

Submitted by Copan Italia Spa (North Attleboro, US). The FDA issued a Cleared decision on August 20, 1997 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2390 - 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.

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Submission Details

510(k) Number K972449 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 1997
Decision Date August 20, 1997
Days to Decision 51 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 102d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSL Culture Media, Anaerobic Transport
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2390
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.