510(k) · Cleared

Cleared

Turbo High-Flow Non-coring Needle

K151341510(k) TraditionalCleared Aug 20, 201593-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

Norfolk Medical · FMI Needle, Hypodermic, Single Lumen

Cleared on Aug 20, 2015 as substantially equivalent to K961088 (Arrow Intl., Inc., 1996) and 1 other predicate after a 93-day review. Its family tree reaches back 1 generation to 1986.

Decided: Aug 20, 2015
Review: 93 days
Class: Class II
Product code: FMI
Recalls: None
Predicates: 2

Its longest line of descent runs back 1 generation to K863721 (1986). 2 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK863721 Norfolk Medical Posi-Grip 'Huber Point' NeedleNorfolk Medical Products, Inc. · 1986
This deviceK151341 Turbo High-Flow Non-coring NeedleNorfolk Medical · 2015

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K863721	Norfolk Medical Posi-Grip 'Huber Point' Needle	Norfolk Medical Products, Inc.	1986	—
0 (this device)	K151341	Turbo High-Flow Non-coring Needle	Norfolk Medical	2015	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1996	1	0

FIG. 1 — Lineage of K151341, 1986–2015Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 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
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (2)

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.

Type	Number	Device	Applicant	Decided	Recalls
*	K961088	Non-Coring Needle Summary page 4 …Needle, Hypodermic Single Lumen, 5.3 Predicate Device Name Device Name: Arrow Non-coring Needle Premarket Notification: K961088 Device Name: Norfolk Medical Posi-Grip Needle Premarket Notification: K863721…	Arrow Intl., Inc.	1996	—
*	K863721	Norfolk Medical Posi-Grip 'Huber Point' Needle Summary page 4 …edle Premarket Notification: K961088 Device Name: Norfolk Medical Posi-Grip Needle Premarket Notification: K863721 1 7350 N. Ridgeway Ÿ Skokie, IL, USA Ÿ 847-674-7075…	Norfolk Medical Products, Inc.	1986	—
†	K111101	Norport CT-PC, Lucent Non-Coring Needel Infusion Set	Norfolk Medical	2011	—

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?

None of the 2 ancestors has a recall.

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. 2015, this device’s year, is highlighted.

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)	—

What is it indicated for?

The Tidal High-Flow Non-coring Needle is intended for the access of totally implantable vascular access ports (VAPs) to

administer I.V. fluids, infusions drugs, and other fluids, and for the administration of blood or blood products, and/or

withdrawal of blood as part of the therapy regimen

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K151341 · printed Nov 6, 2026

Cite this page

510(k) Report. “K151341: Turbo High-Flow Non-coring Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151341

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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