510(k) Report

510(k) · Cleared

Cleared

Dried Gram-Positive Mic/Combo Panels

K993102510(k) TraditionalCleared Dec 2, 199977-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 Dec 2, 1999 as substantially equivalent to K983408 (Dade Microscan, Inc., 1999) after a 77-day review. Its family tree reaches back 1 generation to 1999.

Decided
Dec 2, 1999
Review
77 days
Class
Class II
Product code
LTT
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K983408 (1999). No later device cites it as a predicate yet.

  1. Root · 1 generation backK983408 Dried Gram-Negative and Gram-Positive Mic/Combo PanelsDade Microscan, Inc. · 1999
  2. This deviceK993102 Dried Gram-Positive Mic/Combo PanelsDade Microscan, Inc. · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K983408Dried Gram-Negative and Gram-Positive Mic/Combo PanelsDade Microscan, Inc.1999—
0 (this device)K993102Dried Gram-Positive Mic/Combo PanelsDade Microscan, Inc.1999—
FIG. 1 — Lineage of K993102, 1999–1999Source: 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
*K983408Dried Gram-Negative and Gram-Positive Mic/Combo Panels
Summary page 1
…ded Use: To determine microbial susceptibility to Synercid 510(k) Notification: New antimicrobial - Synercid Predicate device: Microscan Dried Panels e.g. Trovafloxacin (K983408) 510(k) Summary: The proposed MicroScan® Dried Gram-Positive MIC/Combo Panel with Synercid demonstrated substantially equivalent…
Dade Microscan, Inc.1999—

What descends from it?

No later submission names this one as a predicate yet.

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.

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?

To determine gram-positive bacterial susceptibility to the antimicrobial agent Synercid.

Organisms with indications for testing include:

FROM THE INDICATION FOR USE SECTION OF THE MANUFACTURER’S PACKAGE INSERT (7-14-99)

Methicillin-susceptible Staphylococcus aureus

Vancomycin resistant Enterococcus faecium

Streptococcus pyogenes (Gp.A)

FROM THE MICROBIOLOGY SECTION OF THE MANUFACTURER’S PACKAGE INSERT (7-14-99).

Streptococcus agalactiae (Gp.B)

Methicillin-resistant Staphylococcus aureus

Staphylococcus epidermidis

The MicroScan® Dried Gram-Positive MIC/Combo Panels with Synercid are not intended for use with SiFeptococcus pneumoniae and viridans streptococcl.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K993102: Dried Gram-Positive Mic/Combo Panels.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K993102

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