510(k) · Cleared

Cleared

IV Administration Sets with 200(micro)m Blood Filter

K143082510(k) TraditionalCleared Jul 24, 2015270-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

B.Braun Medical, Inc. · FPA Set, Administration, Intravascular

Cleared on Jul 24, 2015 as substantially equivalent to K101677 (Hospira, Inc., 2010) after a 270-day review. Its family tree reaches back 3 generations to 2003. 1 of the 7 devices in its family, counting itself, has a Class I recall. 1 later device descends from it.

Decided: Jul 24, 2015
Review: 270 days
Class: Class II
Product code: FPA
Recalls: None
Predicates: 1

Its longest line of descent runs back 3 generations to K030467 (2003). 5 ancestors in all, the oldest K780880 (1978). 1 later device descends from it, 1 citing it directly. 1 of the 7 devices in this family, counting this one, has a Class I recall.

By dateBy generation

Root · 3 generations backK030467 Gravitech TM Flow Controller Primary Set/Gravitech Flow Controller…Iv Medical, Inc. · 2003
2 generations backK063239 Lifeshield Latex-Free Gravitech Flow Controller I.V. Sets, Models…Hospira, Inc. · 2006 · Recalled
1 generation backK101677 Hospira Infusion Blood SetsHospira, Inc. · 2010 · Recalled (Class I)
This deviceK143082 IV Administration Sets with 200(micro)m Blood FilterB.Braun Medical, Inc. · 2015
Descendant · cites it directly · 0 of its ownK213846 Q2 Blood Administration SetsQuest Medical, Inc. · 2022

Class I recalls in this family

K101677 Hospira Infusion Blood Setsdirect predicate · 2010

Most influential descendants

Showing 1 of 1 · See all

K213846Q2 Blood Administration SetsQuest Medical, Inc. · 2022 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−3	K030467	Gravitech TM Flow Controller Primary Set/Gravitech Flow Controller Extension Set	Iv Medical, Inc.	2003	—
−2	K063239	Lifeshield Latex-Free Gravitech Flow Controller I.V. Sets, Models 17528…	Hospira, Inc.	2006	7
−1	K101677	Hospira Infusion Blood Sets	Hospira, Inc.	2010	Class I
0 (this device)	K143082	IV Administration Sets with 200(micro)m Blood Filter	B.Braun Medical, Inc.	2015	—
+1	K213846	Q2 Blood Administration Sets	Quest Medical, Inc.	2022	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1978	1	0
2003	1	0

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2022	1	0

FIG. 1 — Lineage of K143082, 2003–2022Source: 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.

1 device in this family has a Class I recall. 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

#1 K243841 Sparta Infusion Set for Insulinscore 13.4 · 3 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against? (1)

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
*	K101677	Hospira Infusion Blood Sets Summary page 4 …th 200µm Blood Filter CLASSIFICATION: Class II, Product Code FPA, 880.5440 PREDICATE DEVICE: Hospira Infusion Blood Sets, Hospira Inc., K101677, Class II, FPA, 880.5440 REFERENCE DEVICE: Modified Blood Administration Sets, Baxter Healthcar…	Hospira, Inc.	2010	Class I
†	K993120	Modified Blood Recipient Set	Baxter Healthcare Corp	1999	10

Also cleared against K101677: 7 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K213846	Q2 Blood Administration Sets	Quest Medical, Inc.	2022	0

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

K101677Hospira Infusion Blood SetsHospira, Inc. · 2010 · Direct predicate · ◆ on the line of descent in FIG. 18 Class I recalls

What does this lineage say?

The line of descent spans 12 years and passes through 3 companies; a new generation was cleared every 3.7 years on median.
4 of the 5 ancestors have a recall of any class; 1 has a Class I recall.
Of its descendants, K213846 (Quest Medical, Inc., 2022) has gone furthest, with 0 descendants of its own.
7 other devices also cite its predicate K101677.

How does its category compare?

All FPA devices

FPA Set, Administration, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

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)	—

What is it indicated for?

The IV Administration Sets with 200μm Blood Filter are used to deliver blood, blood components, and IV fluids from a container to a patient's vascular system. When the hand pump component is activated, the device is intended to deliver blood, blood products and crystalloid and colloid resuscitative fluids. These devices may be used for any patient population with consideration given to adequacy of vascular anatomy and appropriateness for the solution being infused and the duration of therapy.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K143082 · printed Nov 6, 2026

Cite this page

510(k) Report. “K143082: IV Administration Sets with 200(micro)m Blood Filter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K143082

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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