510(k) Report

510(k) · Cleared

Cleared

Reliance Endoscope Processing System

K200989510(k) SpecialCleared May 14, 202029-day reviewClass II21 CFR 876.1500

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

STERIS Corporation · NZA Accessories, Germicide, Cleaning, For Endoscopes

Cleared on May 14, 2020 as substantially equivalent to K102244 (STERIS Corporation, 2010) after a 29-day review. Its family tree reaches back 2 generations to 2004. 2 later devices descend from it.

Decided
May 14, 2020
Review
29 days
Class
Class II
Product code
NZA
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K040049 (2004). 2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2021: 1 descendant cleared2022: 1 descendant clearedK040049 · The Reliance Endoscope Processing System · STERIS Corporation · 2004 · recalledK102244 · Reliance Endoscope Processing System · STERIS Corporation · 2010 · recalled200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 1 descendant K102244 · Reliance Endoscope Processing System · STERIS Corporation · 2010 · recalledK040049 · The Reliance Endoscope Processing System · STERIS Corporation · 2004 · recalled0
  1. Root · 2 generations backK040049 The Reliance Endoscope Processing SystemSTERIS Corporation · 2004 · Recalled
  2. 1 generation backK102244 Reliance Endoscope Processing SystemSTERIS Corporation · 2010 · Recalled
  3. This deviceK200989 Reliance Endoscope Processing SystemSTERIS Corporation · 2020
  4. Descendant · cites it directly · 1 of its ownK203223 Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSteris · 2021
  5. Descendant · 2 generations on · 0 of its ownK220361 Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSTERIS Corporation · 2022

Most influential descendants

Showing 2 of 2 · See all
  • K203223Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSteris · 2021 · cites it directly1descendant
  • K220361Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSTERIS Corporation · 2022 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K040049The Reliance Endoscope Processing SystemSTERIS Corporation20042
−1K102244Reliance Endoscope Processing SystemSTERIS Corporation20101
0 (this device)K200989Reliance Endoscope Processing SystemSTERIS Corporation2020—
+1K203223Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSteris2021—
+2K220361Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSTERIS Corporation2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202210
FIG. 1 — Lineage of K200989, 2004–2022Source: 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 NZA? 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 NZA device

  1. #1 K230560 enspire 300 Series Automated Endoscope…score 9.6 · 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
*K102244Reliance Endoscope Processing System
Summary page 5
…Cleaning, For Endoscopes Classification Number: 21 CFR 876.1500 Product Code: NZA 2. Predicate Device Reliance Endoscope Processing System, K102244 3. Description of Device The Reliance Endoscope Processing System is a high level disinfection system that can was…
STERIS Corporation20101

Also cleared against K102244: 2 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K203223Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSteris20211

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?

  • The line of descent spans 16 years and passes through 1 company; a new generation was cleared every 9.4 years on median.
  • 2 of the 2 ancestors have a recall of any class.
  • Of its descendants, K203223 (Steris, 2021) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K102244.

How does its category compare?

All NZA devices

NZA Accessories, Germicide, Cleaning, For Endoscopes: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NZA

2in 2023

2010: 12011: 12013: 12020: 12021: 12022: 12023: 2
2007high 2 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NZA

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

Recalls per year · NZA

No recall names NZA since 2007.

Adverse event reports per year · NZA

2in 2022

2010: 12011: 12012: 142013: 112014: 62015: 102016: 212017: 92018: 82019: 22020: 12021: 42022: 2
2007high 21 (2016) · low 0 (2007)2025

MAUDE reports naming product code NZA, 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
20101—01
20111—01
20120—014
20131—011
20140—06
20150—010
20160—021
20170—09
20180—08
20190—02
20201—01
20211—04
20221—02
20232—00
20240—00
20250—00
20260—0—

What is it indicated for?

The Reliance Endoscope Processing System is intended for washing and high level disinfection of up to two manually pre-cleaned, immersible, reusable, heat-sensitive, semi-critical devices such as GI flexible endoscopes, bronchoscopes and their accessories. High level disinfection is achieved within the 50 – 57°C HLD Phase of the endoscope processing cycle (4 minute generation sequence followed by the 6-minute exposure sequence).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200989: Reliance Endoscope Processing System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200989

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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