Cleared Traditional

K963107 - ETEST FOR CEFEPIME

K963107 is the FDA 510(k) clearance for ETEST FOR CEFEPIME by Ab Biodisk. It is a Class 2 Microbiology device (product code JWY) cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K963107 · Ab Biodisk · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1996
Decision
73d
Days
Class 2
Risk

K963107 is an FDA 510(k) clearance for the ETEST FOR CEFEPIME. Classified as Manual Antimicrobial Susceptibility Test Systems (product code JWY), Class II - Special Controls.

Submitted by Ab Biodisk (Solna, SE). The FDA issued a Cleared decision on October 24, 1996 after a review of 73 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.1640 - 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 Ab Biodisk devices

Submission Details

510(k) Number K963107 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 1996
Decision Date October 24, 1996
Days to Decision 73 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
29d faster than avg
Panel avg: 102d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JWY Manual Antimicrobial Susceptibility Test Systems
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.1640
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 - JWY Manual Antimicrobial Susceptibility Test Systems

All 360
Devices cleared under the same product code (JWY) and FDA review panel - the closest regulatory comparables to K963107.
ETEST SPARFLOXACIN
K970820 · Ab Biodisk · Apr 1997
STREPTOCOCCUS MIC PANEL
K963641 · Dade Microscan, Inc. · Dec 1996
PIPERACILLIN/TAZOBACTAM 4
K964203 · Ab Biodisk · Dec 1996
ETEST SUBMISSION FOR AMOXICILLIN
K960991 · Ab Biodisk · Oct 1996
ETEST FOR AZTREONAM
K962794 · Ab Biodisk · Aug 1996
ETEST SUBMISSION FOR CEFOTETAN
K961517 · Ab Biodisk · Jul 1996