510(k) · Cleared

Cleared

Intraosseous Access Needle

K915409510(k) TraditionalCleared Mar 4, 199293-day reviewClass II21 CFR 880.5570

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

Cook, Inc. · FMI Needle, Hypodermic, Single Lumen

Cleared on Mar 4, 1992 after a 93-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 20 later devices descend from it.

Decided: Mar 4, 1992
Review: 93 days
Class: Class II
Product code: FMI
Recalls: None
Predicates: 0

20 later devices descend from it, 3 citing it directly.

This deviceK915409 Intraosseous Access NeedleCook, Inc. · 1992
Descendant · cites it directly · 17 of its ownK022415 Bone Injection Gun (B.I.G.) for Pediatrics, Model 1STWaismed, Ltd. · 2002
Descendant · 2 generations on · 16 of its ownK043490 PD-IO Disposable Intraosseous Infusion NeedleVidacare Corporation · 2005
Descendant · 3 generations on · 13 of its ownK052195 EZ-Mio Manual DriverVidacare Corporation · 2005
Descendant · cites it directly · 7 of its ownK970380 F.a.S.T. 1 Intraosseous Infusion SystemPyng Medical Corp. · 1997
Descendant · 2 generations on · 4 of its ownK072487 FAST1 Intraosseous Infusion SystemPyng Medical Corp. · 2008

Showing 5 of 20 descendants. See all descendants

Descendants cleared per year

1997high 3 (2005) · low 0 (1998)2026

Most influential descendants

Showing 5 of 20 · See all

K022415Bone Injection Gun (B.I.G.) for Pediatrics, Model 1STWaismed, Ltd. · 2002 · cites it directly17descendants
K043490PD-IO Disposable Intraosseous Infusion NeedleVidacare Corporation · 2005 · 2 generations on16descendants
K052195EZ-Mio Manual DriverVidacare Corporation · 2005 · 3 generations on13descendants
K970380F.a.S.T. 1 Intraosseous Infusion SystemPyng Medical Corp. · 1997 · cites it directly7descendants
K072487FAST1 Intraosseous Infusion SystemPyng Medical Corp. · 2008 · 2 generations on4descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K915409	Intraosseous Access Needle	Cook, Inc.	1992	—
+1	K022415	Bone Injection Gun (B.I.G.) for Pediatrics, Model 1ST	Waismed, Ltd.	2002	—
+2	K043490	PD-IO Disposable Intraosseous Infusion Needle	Vidacare Corporation	2005	—
+3	K052195	EZ-Mio Manual Driver	Vidacare Corporation	2005	—
+1	K970380	F.a.S.T. 1 Intraosseous Infusion System	Pyng Medical Corp.	1997	—
+2	K072487	FAST1 Intraosseous Infusion System	Pyng Medical Corp.	2008	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1997	1	0
2002	1	0
2005	3	0
2006	3	0
2007	1	0
2008	2	0
2009	1	0
2010	2	0
2012	1	0
2013	1	0
2014	1	0
2018	1	0
2019	1	0
2021	1	0

FIG. 1 — Lineage of K915409, 1992–2021Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FMI? 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 FMI device

#1 K252886 Pen Needlescore 14.5 · 4 generations · no Class I recall
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What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (20)

See all 20

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

Number	Device	Applicant	Decided	Descendants
K022415	Bone Injection Gun (B.I.G.) for Pediatrics, Model 1ST	Waismed, Ltd.	2002	17
K970380	F.a.S.T. 1 Intraosseous Infusion System	Pyng Medical Corp.	1997	7
K132583	EZ-IO Intraosseous Infusion System	Vidacare Corporation	2014	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, K022415 (Waismed, Ltd., 2002) has gone furthest, with 17 descendants of its own.

How does its category compare?

All FMI devices

FMI Needle, Hypodermic, Single Lumen: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FMI

11in 2025

2007high 23 (2022) · low 3 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMI

141in 2025

2007high 263 (2020) · low 71 (2007)2026

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

Recalls per year · FMI

1in 2024

2007high 79 (2010) · low 0 (2016)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FMI

2,424in 2025

2007high 4,986 (2023) · low 177 (2008)2025

MAUDE reports naming product code FMI, 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	15	71	2	208
2008	10	85	4	177
2009	7	177	3	263
2010	15	119	79	249
2011	12	113	5	240
2012	17	107	1	215
2013	11	87	1	255
2014	14	155	3	287
2015	10	89	1	567
2016	20	217	0	941
2017	9	253	16	1,547
2018	20	176	0	2,398
2019	12	186	5	4,896
2020	11	263	3	4,245
2021	18	143	7	4,532
2022	23	189	0	4,885
2023	18	112	2	4,986
2024	3	90	1	4,053
2025	11	141	0	2,424
2026	12	119	1 (1)	—

https://510kreport.com/device/K915409 · printed Nov 6, 2026

Cite this page

510(k) Report. “K915409: Intraosseous Access Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K915409

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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