510(k) · Cleared

Cleared

Heavy-Duty I.V. Stand

K823270510(k) TraditionalCleared Nov 17, 198215-day reviewClass I21 CFR 880.6990

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

Cleared on Nov 17, 1982 after a 15-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided: Nov 17, 1982
Review: 15 days
Class: Class I
Product code: FOX
Recalls: None
Predicates: 0

2 later devices descend from it, 2 citing it directly.

This deviceK823270 Heavy-Duty I.V. StandE.F. Brewer Co. · 1982
Descendant · cites it directly · 0 of its ownK980336 IV StandsClinton Industries, Inc. · 1998
Descendant · cites it directly · 0 of its ownK964782 Medrad Contrast HolderMedrad, Inc. · 1997

Most influential descendants

Showing 2 of 2 · See all

K980336IV StandsClinton Industries, Inc. · 1998 · cites it directly0descendants
K964782Medrad Contrast HolderMedrad, Inc. · 1997 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K823270	Heavy-Duty I.V. Stand	E.F. Brewer Co.	1982	—
+1	K980336	IV Stands	Clinton Industries, Inc.	1998	—
+1	K964782	Medrad Contrast Holder	Medrad, Inc.	1997	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1997	1	0
1998	1	0

FIG. 1 — Lineage of K823270, 1982–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 FOX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Candidate predicates for a device like this, rankedin the report
Recall history across each candidate’s familyin the report

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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? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K980336	IV Stands	Clinton Industries, Inc.	1998	0
K964782	Medrad Contrast Holder	Medrad, Inc.	1997	0

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, K980336 (Clinton Industries, Inc., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FOX devices

FOX Stand, Infusion: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FOX

FDA has decided no FOX device since 2007.

Median 510(k) review, days · FOX

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

Recalls per year · FOX

1in 2016

2007high 1 (2015) · low 0 (2007)2026

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

Adverse event reports per year · FOX

2in 2025

2007high 173 (2021) · low 2 (2009)2025

MAUDE reports naming product code FOX, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	—	0	4
2008	—	0	3
2009	—	0	2
2010	—	0	3
2011	—	0	10
2012	—	0	5
2013	—	0	7
2014	—	0	2
2015	—	1	3
2016	—	1	2
2017	—	0	8
2018	—	0	17
2019	—	0	23
2020	—	0	112
2021	—	0	173
2022	—	0	12
2023	—	0	3
2024	—	0	6
2025	—	0	2
2026	—	0	—

https://510kreport.com/device/K823270 · printed Nov 6, 2026

Cite this page

510(k) Report. “K823270: Heavy-Duty I.V. Stand.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K823270

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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