510(k) · Cleared

Cleared

Flu Ven I.V. Set 0153-C Perma-Set

K843692510(k) TraditionalCleared Oct 31, 198442-day reviewClass II21 CFR 880.5440

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

Venusa, Ltd. · FPA Set, Administration, Intravascular

Cleared on Oct 31, 1984 after a 42-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: Oct 31, 1984
Review: 42 days
Class: Class II
Product code: FPA
Recalls: None
Predicates: 0

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

This deviceK843692 Flu Ven I.V. Set 0153-C Perma-SetVenusa, Ltd. · 1984
Descendant · cites it directly · 0 of its ownK082027 Flu-Admin, Models 60150, 60150C, 60151C, 60153C, 60160Genesis Bps, LLC · 2009
Descendant · cites it directly · 0 of its ownK042129 F00010 - IV Gravity Setwith Male Luer Slip; F00027 - IV Gravity Set…Cedic S.R.L. · 2005

Most influential descendants

Showing 2 of 2 · See all

K082027Flu-Admin, Models 60150, 60150C, 60151C, 60153C, 60160Genesis Bps, LLC · 2009 · cites it directly0descendants
K042129F00010 - IV Gravity Setwith Male Luer Slip; F00027 - IV Gravity Set with Male Luer LockCedic S.R.L. · 2005 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K843692	Flu Ven I.V. Set 0153-C Perma-Set	Venusa, Ltd.	1984	—
+1	K082027	Flu-Admin, Models 60150, 60150C, 60151C, 60153C, 60160	Genesis Bps, LLC	2009	—
+1	K042129	F00010 - IV Gravity Setwith Male Luer Slip; F00027 - IV Gravity Set with Male…	Cedic S.R.L.	2005	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2005	1	0
2009	1	0

FIG. 1 — Lineage of K843692, 1984–2009Source: 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 FPA? 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 FPA device

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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
K082027	Flu-Admin, Models 60150, 60150C, 60151C, 60153C, 60160	Genesis Bps, LLC	2009	0
K042129	F00010 - IV Gravity Setwith Male Luer Slip; F00027 - IV Gravity Set with Male Luer Lock	Cedic S.R.L.	2005	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, K082027 (Genesis Bps, LLC, 2009) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FPA devices

FPA Set, Administration, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FPA

11in 2025

2007high 23 (2010) · low 4 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FPA

225in 2025

2007high 340 (2023) · low 75 (2007)2026

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

Recalls per year · FPA

98in 2025

2007high 166 (2009) · low 1 (2021)2026

Class I (17 since 2007) Class II/III not classified

Adverse event reports per year · FPA

34,506in 2025

2007high 47,210 (2024) · low 1,499 (2007)2025

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

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	16	75	17	1,499
2008	18	89	15	1,941
2009	10	166	166	2,512
2010	23	120	58	2,537
2011	12	87	28	4,407
2012	21	96	16 (4)	4,930
2013	13	90	64	4,651
2014	22	89	24	4,695
2015	17	123	6	6,625
2016	12	195	10	8,470
2017	17	240	13	6,462
2018	4	177	4	6,574
2019	7	161	13	11,227
2020	10	327	107	9,563
2021	13	186	1	10,414
2022	14	213	9 (5)	13,393
2023	14	340	12 (4)	10,916
2024	7	244	13 (1)	47,210
2025	11	225	98 (1)	34,506
2026	5	266	10 (2)	—

https://510kreport.com/device/K843692 · printed Nov 5, 2026

Cite this page

510(k) Report. “K843692: Flu Ven I.V. Set 0153-C Perma-Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K843692

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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