510(k) Report

510(k) · Cleared

Cleared

Joslyn EO Sterilizer/ EO Modernization Kit

K901146510(k) TraditionalCleared Mar 7, 1991360-day reviewClass II21 CFR 880.6860

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

Joslyn Valve Corp. · FLF Sterilizer, Ethylene-Oxide Gas

Cleared on Mar 7, 1991 after a 360-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Mar 7, 1991
Review
360 days
Class
Class II
Product code
FLF
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared1990200020102020
  1. This deviceK901146 Joslyn EO Sterilizer/ EO Modernization KitJoslyn Valve Corp. · 1991
  2. Descendant · cites it directly · 0 of its ownK014013 H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC · 2003

Most influential descendants

Showing 1 of 1 · See all
  • K014013H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K901146Joslyn EO Sterilizer/ EO Modernization KitJoslyn Valve Corp.1991—
+1K014013H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K901146, 1991–2003Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FLF? 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 FLF device

  1. #1 K192978 EOGas 4 Ethylene Oxide Gas Sterilizerscore 0.6 · 2 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K014013H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC20030

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?

  • Of its descendants, K014013 (H & W Technology, LLC, 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FLF devices

FLF Sterilizer, Ethylene-Oxide Gas: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FLF

1in 2020

2009: 12015: 22017: 12020: 1
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLF

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

Recalls per year · FLF

2in 2014

2009: 12012: 12013: 22014: 2
2007high 2 (2013) · low 0 (2007)2026

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

Adverse event reports per year · FLF

4in 2021

2007: 22008: 12009: 22010: 32011: 42012: 52013: 32014: 62015: 32016: 32017: 32019: 22021: 4
2007high 6 (2014) · low 0 (2018)2025

MAUDE reports naming product code FLF, 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—02
20080—01
20091—12
20100—03
20110—04
20120—15
20130—23
20140—26
20152—03
20160—03
20171—03
20180—00
20190—02
20201—00
20210—04
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K901146: Joslyn EO Sterilizer/ EO Modernization Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K901146

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026