510(k) Report

510(k) · Cleared

Cleared

H & W Hospital Ethylene Oxide Sterilizer Control System

K014013510(k) AbbreviatedCleared Jun 25, 2003567-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

H & W Technology, LLC · FLF Sterilizer, Ethylene-Oxide Gas

Cleared on Jun 25, 2003 as substantially equivalent to K901146 (Joslyn Valve Corp., 1991) after a 567-day review. Its family tree reaches back 1 generation to 1991.

Decided
Jun 25, 2003
Review
567 days
Class
Class II
Product code
FLF
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K901146 (1991). No later device cites it as a predicate yet.

K901146 · Joslyn EO Sterilizer/ EO Modernization Kit · Joslyn Valve Corp. · 19911990199520002005
  1. Root · 1 generation backK901146 Joslyn EO Sterilizer/ EO Modernization KitJoslyn Valve Corp. · 1991
  2. This deviceK014013 H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC · 2003
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K901146Joslyn EO Sterilizer/ EO Modernization KitJoslyn Valve Corp.1991—
0 (this device)K014013H & W Hospital Ethylene Oxide Sterilizer Control SystemH & W Technology, LLC2003—
FIG. 1 — Lineage of K014013, 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), 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 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
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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
*K901146Joslyn EO Sterilizer/ EO Modernization Kit
Summary page 1
…formance standards) (as per 21CFR, part 880.6860 equivalent device) Legally Marketed Equivalent Device Name(s) Joslyn EO Sterilizer/EO Modernization Kit (K901146) Description of Device This device is an accessory to an electronic ethylene oxide sterilizer control system. This control syst…
Joslyn Valve Corp.1991—

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 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—

What is it indicated for?

The H & W Hospital Ethylene Oxide Sterilizer Control System is an accessory in the form of an electronic control system for the retrofit of existing sterilizers to provide operator and information monitoring capabilities of a personal computer (PC) together with the functional reliability, safety, and dependability of control obtained through the use of a programmable logic controller (PLC). The H & W Hospital Ethylene Oxide Sterilizer Control System is…

Read the full statement (140 words)

The H & W Hospital Ethylene Oxide Sterilizer Control System is an accessory in the form of an electronic control system for the retrofit of existing sterilizers to provide operator and information monitoring capabilities of a personal computer (PC) together with the functional reliability, safety, and dependability of control obtained through the use of a programmable logic controller (PLC). The H & W Hospital Ethylene Oxide Sterilizer Control System is intended to retrofit existing Steris (Amsco) Eagle Model 2000 & 3000 series and Getinge (Castle) Model M/C 3500, 3600 or 4200 series Hospital EO Sterilizers only. The automated cycle performs in such a manner as to assure the repeatability of the process. The predetermined cycles duplicate the cycles provided by the original equipment manufacturer and are demonstrated to deliver the biological performance as stipulated in the consensus standard ANSI/AAMI ST-24.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K014013: H & W Hospital Ethylene Oxide Sterilizer Control System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K014013

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026