510(k) Report

510(k) · Cleared

Cleared

Decanter Models-Various

K830232510(k) TraditionalCleared Feb 9, 198315-day reviewClass II21 CFR 880.5025

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

Steri-Sytems, Corp. · KPE Container, I.V.

Cleared on Feb 9, 1983 after a 15-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
Feb 9, 1983
Review
15 days
Class
Class II
Product code
KPE
Recalls
None
Predicates
0

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

Descendants, by year cleared 2002: 1 descendant cleared19801990200020102020
  1. This deviceK830232 Decanter Models-VariousSteri-Sytems, Corp. · 1983
  2. Descendant · cites it directly · 0 of its ownK023539 Steri-Spouts; Bag-Spout, Vial-Spout, Transfer Mixer; Rapidflow…Valumed · 2002

Most influential descendants

Showing 1 of 1 · See all
  • K023539Steri-Spouts; Bag-Spout, Vial-Spout, Transfer Mixer; Rapidflow, Vialflow, TransflowValumed · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K830232Decanter Models-VariousSteri-Sytems, Corp.1983—
+1K023539Steri-Spouts; Bag-Spout, Vial-Spout, Transfer Mixer; Rapidflow, Vialflow…Valumed2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K830232, 1983–2002Source: 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 KPE? 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 KPE device

  1. #1 K223674 eZSURE™ Empty Fluid Container (models 426030…score 13.1 · 5 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?

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
K023539Steri-Spouts; Bag-Spout, Vial-Spout, Transfer Mixer; Rapidflow, Vialflow, TransflowValumed20020

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, K023539 (Valumed, 2002) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KPE devices

KPE Container, I.V.: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KPE

2in 2025

2008: 12009: 12011: 22012: 12013: 12019: 32020: 12021: 22023: 22024: 12025: 22026 (partial year): 3
2007high 3 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPE

183in 2019

2019: 183 days median2026 (partial year): 270 days median
2007high 270 (2026) · low 183 (2019)2026

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

Recalls per year · KPE

16in 2024

2009: 32010: 142014: 2, 2 Class I2017: 12018: 132022: 22024: 16
2007high 16 (2024) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · KPE

220in 2025

2007: 432008: 222009: 382010: 872011: 7972012: 1,2292013: 6222014: 5752015: 5432016: 5272017: 2842018: 1422019: 2052020: 1472021: 1622022: 1122023: 1272024: 1582025: 220
2007high 1,229 (2012) · low 22 (2008)2025

MAUDE reports naming product code KPE, 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—043
20081—022
20091—338
20100—1487
20112—0797
20121—01,229
20131—0622
20140—2 (2)575
20150—0543
20160—0527
20170—1284
20180—13142
201931830205
20201—0147
20212—0162
20220—2112
20232—0127
20241—16158
20252—0220
202632700—
Cite this page

510(k) Report. “K830232: Decanter Models-Various.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K830232

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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