Cleared Traditional

K896278 - SCEPTOR - NEW ANTIMICROBIAL AGENT - CEF...

K896278 is the FDA 510(k) clearance for SCEPTOR - NEW ANTIMICROBIAL AGENT - CEF... by Bd Becton Dickinson Vacutainer Systems Preanalytic. It is a Class 2 Microbiology device (product code JWY) cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K896278 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Microbiology device
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Mar 1990
Decision
127d
Days
Class 2
Risk

K896278 is an FDA 510(k) clearance for the SCEPTOR - NEW ANTIMICROBIAL AGENT - CEFOTETAN. Classified as Manual Antimicrobial Susceptibility Test Systems (product code JWY), Class II - Special Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lakes, US). The FDA issued a Cleared decision on March 7, 1990 after a review of 127 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Bd Becton Dickinson Vacutainer Systems Preanalytic devices

Submission Details

510(k) Number K896278 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 31, 1989
Decision Date March 07, 1990
Days to Decision 127 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d slower than avg
Panel avg: 102d · This submission: 127d
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 366
Devices cleared under the same product code (JWY) and FDA review panel - the closest regulatory comparables to K896278.
EF SYNERGY QUAD MODIFIED
K910242 · Remel Co. · Mar 1991
EF SYNERGY QUAD
K903589 · Remel Co. · Nov 1990
PASCO MIC AND MIC/ID MODIFIED
K902739 · Pasco Laboratories, Inc. · Jul 1990
MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE
K896566 · Medical Specialties, Inc. · Feb 1990
PASCO MIC/ID GRAM-POSITIVE PANEL
K895215 · Difco Laboratories, Inc. · Jan 1990
API UNISCEPT KB
K895796 · Analytical Products, Inc. · Nov 1989