510(k) Report

510(k) · Cleared

Cleared

Microscan Microstrep Plus Panel New Antimicrobial - Cefotaxime

K021111510(k) TraditionalCleared Jun 6, 200262-day reviewClass II21 CFR 866.1640

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Dade Microscan, Inc. · LTT Panels, Test, Susceptibility, Antimicrobial

Cleared on Jun 6, 2002 as substantially equivalent to K963641 (Dade Microscan, Inc., 1996) after a 62-day review. Its family tree reaches back 1 generation to 1996. 1 later device descends from it.

Decided
Jun 6, 2002
Review
62 days
Class
Class II
Product code
LTT
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K963641 (1996). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2006: 1 descendant clearedK963641 · Streptococcus Mic Panel · Dade Microscan, Inc. · 19961995200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant K963641 · Streptococcus Mic Panel · Dade Microscan, Inc. · 19960
  1. Root · 1 generation backK963641 Streptococcus Mic PanelDade Microscan, Inc. · 1996
  2. This deviceK021111 Microscan Microstrep Plus Panel New Antimicrobial - CefotaximeDade Microscan, Inc. · 2002
  3. Descendant · cites it directly · 0 of its ownK063101 Microscan Microstrep Plus Panel Cefotaxime (0.015 - 8 MCG/MLDade Behring, Inc. · 2006

Most influential descendants

Showing 1 of 1 · See all
  • K063101Microscan Microstrep Plus Panel Cefotaxime (0.015 - 8 MCG/MLDade Behring, Inc. · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K963641Streptococcus Mic PanelDade Microscan, Inc.1996—
0 (this device)K021111Microscan Microstrep Plus Panel New Antimicrobial - CefotaximeDade Microscan, Inc.2002—
+1K063101Microscan Microstrep Plus Panel Cefotaxime (0.015 - 8 MCG/MLDade Behring, Inc.2006—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K021111, 1996–2006Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LTT? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LTT device

  1. #1 K243804 MicroScan Dried Gram-Negative MIC/Combo Panels…score 10.8 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K963641Streptococcus Mic Panel
Summary page 1
…bilitywith aerobic streptococci,including Streptococcuspneumoniae Predicate device: Microscan@StreptococcusMZC Panel 6963641). 510(k) Summary: The Microscan@MlCroSTREPpZusT” Panel is used to determine quantitative andor qualitative antim…
Dade Microscan, Inc.1996—

Also cleared against K963641: 21 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K063101Microscan Microstrep Plus Panel Cefotaxime (0.015 - 8 MCG/MLDade Behring, Inc.20060

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • Of its descendants, K063101 (Dade Behring, Inc., 2006) has gone furthest, with 0 descendants of its own.
  • 21 other devices also cite its predicate K963641.

How does its category compare?

All LTT devices

LTT Panels, Test, Susceptibility, Antimicrobial: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LTT

3in 2025

2009: 22010: 12011: 12013: 22015: 12017: 42019: 12020: 42025: 3
2007high 4 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LTT

219in 2025

2017: 132 days median2020: 90 days median2025: 219 days median
2007high 219 (2025) · low 90 (2020)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LTT

7in 2015

2015: 7
2007high 7 (2015) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LTT

3in 2017

2007: 72008: 42009: 12010: 12011: 12013: 52014: 92015: 102016: 12017: 3
2007high 10 (2015) · low 0 (2012)2025

MAUDE reports naming product code LTT, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—07
20080—04
20092—01
20101—01
20111—01
20120—00
20132—05
20140—09
20151—710
20160—01
2017413203
20180—00
20191—00
202049000
20210—00
20220—00
20230—00
20240—00
2025321900
20260—0—

What is it indicated for?

The MicroScan® MICroSTREP plus™ Panel is used to determine quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including Streptococcus pneumoniae. After inoculation, panels are incubated for 20 - 24 hours at 35°C +/- 1°C in a non-CO2 incubator, and read visually according to the Package Insert. This particular submission is for the addition of the antimicrobial Cefotaxime at…

Read the full statement (105 words)

The MicroScan® MICroSTREP plus™ Panel is used to determine quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including Streptococcus pneumoniae. After inoculation, panels are incubated for 20 - 24 hours at 35°C +/- 1°C in a non-CO2 incubator, and read visually according to the Package Insert.

This particular submission is for the addition of the antimicrobial Cefotaxime at concentrations of 0.015 to 8 mcg/ml to the test panel

The organisms which may be used for Cefotaxime susceptibility testing in this panel are:

Streptococcus pyogenes (Group A beta-hemolytic streptococci)

Streptococcus agalactiae (Group B streptococci)

Streptococcus pneumoniae (formerly Diplococcus pneumoniae)

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K021111: Microscan Microstrep Plus Panel New Antimicrobial - Cefotaxime.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K021111

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026