Cleared Traditional

K261781 - Thermo Scientific Oxoid Cefepime/Zideba...

K261781 is the FDA 510(k) clearance for Thermo Scientific Oxoid Cefepime/Zideba... by Thermo Fisher Scientific (Oxoid Ltd.). It is a Class 2 Microbiology device (product code JTN) cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K261781 · Thermo Fisher Scientific (Oxoid Ltd.) · Microbiology device
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Jul 2026
Decision
56d
Days
Class 2
Risk

K261781 is an FDA 510(k) clearance for the Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60. Classified as Susceptibility Test Discs, Antimicrobial (product code JTN), Class II - Special Controls.

Submitted by Thermo Fisher Scientific (Oxoid Ltd.) (Basingstoke, GB). The FDA issued a Cleared decision on July 24, 2026 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.1620 - 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 Thermo Fisher Scientific (Oxoid Ltd.) devices

Submission Details

510(k) Number K261781 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 29, 2026
Decision Date July 24, 2026
Days to Decision 56 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 102d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JTN Susceptibility Test Discs, Antimicrobial
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.1620
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 - JTN Susceptibility Test Discs, Antimicrobial

All 283
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