510(k) Report

510(k) · Cleared

Cleared

Bblcrystal Neisseria/Haemophilus (N/H) System

K962423510(k) TraditionalCleared Aug 2, 199639-day reviewClass I21 CFR 866.2660

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

Becton Dickinson Microbiology Systems · JST Kit, Fastidious Organisms

Cleared on Aug 2, 1996 as substantially equivalent to K881501 (Innovative Diagnostic Systems, Inc., 1988) after a 39-day review. Its family tree reaches back 1 generation to 1988.

Decided
Aug 2, 1996
Review
39 days
Class
Class I
Product code
JST
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K881501 (1988). No later device cites it as a predicate yet.

K881501 · Modified Ids Rapid NH System · Innovative Diagnostic Systems, Inc. · 19881986198819901992199419961998
  1. Root · 1 generation backK881501 Modified Ids Rapid NH SystemInnovative Diagnostic Systems, Inc. · 1988
  2. This deviceK962423 Bblcrystal Neisseria/Haemophilus (N/H) SystemBecton Dickinson Microbiology Systems · 1996
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K881501Modified Ids Rapid NH SystemInnovative Diagnostic Systems, Inc.1988—
0 (this device)K962423Bblcrystal Neisseria/Haemophilus (N/H) SystemBecton Dickinson Microbiology Systems1996—
FIG. 1 — Lineage of K962423, 1988–1996Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

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  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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
*K881501Modified Ids Rapid NH System
Summary page 1
…Classification Name: Microbiology - Discs, Strips, and Reagents, Microorganism Differentiation PREDICATE DEVICES: Innovative Diagnostic Systems, Inc., RapID™ NH System (K881501) DEVICE DESCRIPTION: INTENDED USE: The BBLCRYSTAL™ Nelsseria/Haemophilus (N/H) Identification (ID) System is a miniaturized iden…
Innovative Diagnostic Systems, Inc.1988—

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 JST devices

JST Kit, Fastidious Organisms: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JST

FDA has decided no JST device since 2007.

Median 510(k) review, days · JST

Too few JST 510(k)s in any year since 2007 to give a median.

Recalls per year · JST

3in 2022

2022: 3
2007high 3 (2022) · low 0 (2007)2026

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

Adverse event reports per year · JST

1in 2021

2017: 142018: 92021: 1
2007high 14 (2017) · low 0 (2007)2025

MAUDE reports naming product code JST, 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—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—014
20180—09
20190—00
20200—00
20210—01
20220—30
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

Use of this product is indicated when Neisseria, Haemophilus and the other fastidious organisms described in Table B-1 have been isolated in pure culture from clinical specimens in a clinical laboratory, and identification of the microorganisms is desired.

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. “K962423: Bblcrystal Neisseria/Haemophilus (N/H) System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K962423

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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