Cleared Traditional

K961148 - CEFEPIME DISPANS-O-DISC (CEFEPLIME - 30...

K961148 is the FDA 510(k) clearance for CEFEPIME DISPANS-O-DISC (CEFEPLIME - 30... by Difco Laboratories, Inc.. It is a Class 1 Microbiology device (product code JTW) cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K961148 · Difco Laboratories, Inc. · Microbiology device
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Apr 1996
Decision
36d
Days
Class 1
Risk

K961148 is an FDA 510(k) clearance for the CEFEPIME DISPANS-O-DISC (CEFEPLIME - 30MCG). Classified as System, Transport, Aerobic (product code JTW), Class I - General Controls.

Submitted by Difco Laboratories, Inc. (Livouia, US). The FDA issued a Cleared decision on April 26, 1996 after a review of 36 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2900 - 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 Difco Laboratories, Inc. devices

Submission Details

510(k) Number K961148 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 1996
Decision Date April 26, 1996
Days to Decision 36 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 102d · This submission: 36d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JTW System, Transport, Aerobic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2900
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.

Regulatory Peers - JTW System, Transport, Aerobic

All 13
Devices cleared under the same product code (JTW) and FDA review panel - the closest regulatory comparables to K961148.
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