510(k) Report

510(k) · Cleared

Cleared

Getinge 800HC- Series Steam Sterilizer

K122625510(k) TraditionalCleared May 22, 2013267-day reviewClass II21 CFR 880.6880

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

Getinge Sourcing, LLC · FLE Sterilizer, Steam

Cleared on May 22, 2013 as substantially equivalent to K120441 (Getinge Sourcing, LLC, 2012) after a 267-day review. Its family tree reaches back 6 generations to 1982.

Decided
May 22, 2013
Review
267 days
Class
Class II
Product code
FLE
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K820783 (1982). No later device cites it as a predicate yet.

  1. Root · 6 generations backK820783 Castle Microcomputer Sterilizer ControlSybron Corp. · 1982
  2. 5 generations backK970907 Castle Series 100 Steam Sterilizers (Straightline)Getinge/Castle, Inc. · 1997
  3. 4 generations backK994314 Castle Series 100HC Steam SterilizersGetinge/Castle, Inc. · 2000
  4. 3 generations backK012573 Castle 400HC/500HC Series Steam Sterilizer, Models 422HC, 433HC…Getinge/Castle, Inc. · 2001
  5. 2 generations backK103504 Getinge 400HC/500HC Series Steam SterilizerGetinge Sourcing, LLC · 2011
  6. 1 generation backK120441 Getinge 700HC-E Series Steam SterilizerGetinge Sourcing, LLC · 2012
  7. This deviceK122625 Getinge 800HC- Series Steam SterilizerGetinge Sourcing, LLC · 2013
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K820783Castle Microcomputer Sterilizer ControlSybron Corp.1982—
−5K970907Castle Series 100 Steam Sterilizers (Straightline)Getinge/Castle, Inc.1997—
−4K994314Castle Series 100HC Steam SterilizersGetinge/Castle, Inc.2000—
−3K012573Castle 400HC/500HC Series Steam Sterilizer, Models 422HC, 433HC, 522HC, and…Getinge/Castle, Inc.2001—
−2K103504Getinge 400HC/500HC Series Steam SterilizerGetinge Sourcing, LLC2011—
−1K120441Getinge 700HC-E Series Steam SterilizerGetinge Sourcing, LLC2012—
0 (this device)K122625Getinge 800HC- Series Steam SterilizerGetinge Sourcing, LLC2013—
FIG. 1 — Lineage of K122625, 1982–2013Source: 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 FLE? 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 FLE device

  1. #1 K250168 Life Ultra 25L Tabletop Mono Chamber Steam…score 12.7 · 8 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
*K120441Getinge 700HC-E Series Steam SterilizerGetinge Sourcing, LLC2012—

Also cleared against K120441: 1 other device →

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?

  • The line of descent spans 31 years and passes through 3 companies; a new generation was cleared every 2.3 years on median.
  • None of the 6 ancestors has a recall.
  • 1 other device also cites its predicate K120441.

How does its category compare?

All FLE devices

FLE Sterilizer, Steam: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · FLE

4in 2025

2007: 52008: 12009: 82010: 22011: 52012: 52013: 52014: 22015: 32016: 12017: 32018: 82019: 52020: 22021: 52022: 102023: 72024: 22025: 42026 (partial year): 3
2007high 10 (2022) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLE

184in 2025

2007: 67 days median2009: 109 days median2011: 141 days median2012: 111 days median2013: 241 days median2015: 302 days median2017: 233 days median2018: 146 days median2019: 192 days median2021: 147 days median2022: 133 days median2023: 88 days median2025: 184 days median2026 (partial year): 85 days median
2007high 302 (2015) · low 67 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FLE

1in 2021

2007: 12008: 12011: 12012: 12013: 22015: 12018: 12019: 22021: 12026 (partial year): 1
2007high 2 (2013) · low 0 (2009)2026

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

Adverse event reports per year · FLE

71in 2025

2007: 192008: 212009: 192010: 202011: 632012: 692013: 1122014: 1132015: 682016: 762017: 632018: 902019: 912020: 872021: 812022: 702023: 662024: 642025: 71
2007high 113 (2014) · low 19 (2007)2025

MAUDE reports naming product code FLE, 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
2007567119
20081—121
20098109019
20102—020
20115141163
20125111169
201352412112
20142—0113
20153302168
20161—076
20173233063
20188146190
20195192291
20202—087
20215147181
202210133070
2023788066
20242—064
20254184071
20263851—

What is it indicated for?

The Getinge 800HC-E Series Steam Sterilizer is intended for use by health care facilities to sterilize wrapped and unwrapped, porous and nonporous heat and moisture stable items such as surgical instruments and linens by means of pressurized steam. The 80011C-E Series Steam Sterilizer is available in 2 models differentiated by chamber length; 833HC-E 42 inch chamber and 833HC-E 76 inch chamber.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122625: Getinge 800HC- Series Steam Sterilizer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122625

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