510(k) Report

510(k) · Cleared

Cleared

Surshield Safety Winged Blood Collection Set

K031279510(k) TraditionalCleared May 30, 200338-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

Terumo Medical Products Hangzhou Co., Ltd. · FPA Set, Administration, Intravascular

Cleared on May 30, 2003 as substantially equivalent to K013164 (Terumo Medical Corp., 2001) after a 38-day review. Its family tree reaches back 3 generations to 1997. 3 later devices descend from it.

Decided
May 30, 2003
Review
38 days
Class
Class II
Product code
FPA
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K970259 (1997). 6 ancestors in all, the oldest K931367 (1993). 3 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 1 other ancestor1998: 1 other ancestor1993: 1 other ancestor2020: 1 descendant cleared2005: 1 descendant cleared2015: 1 descendant clearedK970259 · E-Z Set Infusion Set/Saf-T E-Z Set Infusion Set · Becton Dickinson Vascular Access, Inc. · 1997K980414 · Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple, Vacutainer Brand Blood Collection Set · Bd Becton Dickinson Vacutainer Systems Preanalytic · 1998 · recalledK013164 · Surshield Safety Winged Blood Collection Set · Terumo Medical Corp. · 20011990200020102020
  1. Root · 3 generations backK970259 E-Z Set Infusion Set/Saf-T E-Z Set Infusion SetBecton Dickinson Vascular Access, Inc. · 1997
  2. 2 generations backK980414 Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple…Bd Becton Dickinson Vacutainer Systems Preanalytic · 1998 · Recalled
  3. 1 generation backK013164 Surshield Safety Winged Blood Collection SetTerumo Medical Corp. · 2001
  4. This deviceK031279 Surshield Safety Winged Blood Collection SetTerumo Medical Products Hangzhou Co., Ltd. · 2003
  5. Descendant · cites it directly · 0 of its ownK192681 Safety scalp vein set, Scalp vein set, Blood collection needle…Jiangsu Kangbao Medical Equipment Co., Ltd. · 2020
  6. Descendant · cites it directly · 0 of its ownK151991 Safelock Disposable Blood Collection Set, Disposable Blood…Jiangyin Caina Technology Co., Ltd. · 2015
  7. Descendant · cites it directly · 0 of its ownK043328 Microflo-Safe Scalp Vein SetDks Loversan Industria Biomedica Spa · 2005

Most influential descendants

Showing 3 of 3 · See all
  • K192681Safety scalp vein set, Scalp vein set, Blood collection needle (Scalp vein set type)…Jiangsu Kangbao Medical Equipment Co., Ltd. · 2020 · cites it directly0descendants
  • K151991Safelock Disposable Blood Collection Set, Disposable Blood Collection SetJiangyin Caina Technology Co., Ltd. · 2015 · cites it directly0descendants
  • K043328Microflo-Safe Scalp Vein SetDks Loversan Industria Biomedica Spa · 2005 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K970259E-Z Set Infusion Set/Saf-T E-Z Set Infusion SetBecton Dickinson Vascular Access, Inc.1997—
−2K980414Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple, Vacutainer…Bd Becton Dickinson Vacutainer Systems Preanalytic19981
−1K013164Surshield Safety Winged Blood Collection SetTerumo Medical Corp.2001—
0 (this device)K031279Surshield Safety Winged Blood Collection SetTerumo Medical Products Hangzhou Co., Ltd.2003—
+1K192681Safety scalp vein set, Scalp vein set, Blood collection needle (Scalp vein set…Jiangsu Kangbao Medical Equipment Co., Ltd.2020—
+1K151991Safelock Disposable Blood Collection Set, Disposable Blood Collection SetJiangyin Caina Technology Co., Ltd.2015—
+1K043328Microflo-Safe Scalp Vein SetDks Loversan Industria Biomedica Spa2005—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199810
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
201510
202010
FIG. 1 — Lineage of K031279, 1997–2020Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 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

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

TypeNumberDeviceApplicantDecidedRecalls
*K013164Surshield Safety Winged Blood Collection SetTerumo Medical Corp.2001—

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K192681Safety scalp vein set, Scalp vein set, Blood collection needle (Scalp vein set type)…Jiangsu Kangbao Medical Equipment Co., Ltd.20200
K151991Safelock Disposable Blood Collection Set, Disposable Blood Collection SetJiangyin Caina Technology Co., Ltd.20150
K043328Microflo-Safe Scalp Vein SetDks Loversan Industria Biomedica Spa20050

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?

  • The line of descent spans 6 years and passes through 4 companies; a new generation was cleared every 1.6 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K192681 (Jiangsu Kangbao Medical Equipment Co., Ltd., 2020) 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

2007: 162008: 182009: 102010: 232011: 122012: 212013: 132014: 222015: 172016: 122017: 172018: 42019: 72020: 102021: 132022: 142023: 142024: 72025: 112026 (partial year): 5
2007high 23 (2010) · low 4 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FPA

225in 2025

2007: 75 days median2008: 89 days median2009: 166 days median2010: 120 days median2011: 87 days median2012: 96 days median2013: 90 days median2014: 89 days median2015: 123 days median2016: 195 days median2017: 240 days median2018: 177 days median2019: 161 days median2020: 327 days median2021: 186 days median2022: 213 days median2023: 340 days median2024: 244 days median2025: 225 days median2026 (partial year): 266 days median
2007high 340 (2023) · low 75 (2007)2026

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

Recalls per year · FPA

98in 2025

2007: 172008: 152009: 1662010: 582011: 282012: 16, 4 Class I2013: 642014: 242015: 62016: 102017: 132018: 42019: 132020: 1072021: 12022: 9, 5 Class I2023: 12, 4 Class I2024: 13, 1 Class I2025: 98, 1 Class I2026 (partial year): 10, 2 Class I
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

2007: 1,4992008: 1,9412009: 2,5122010: 2,5372011: 4,4072012: 4,9302013: 4,6512014: 4,6952015: 6,6252016: 8,4702017: 6,4622018: 6,5742019: 11,2272020: 9,5632021: 10,4142022: 13,3932023: 10,9162024: 47,2102025: 34,506
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071675171,499
20081889151,941
2009101661662,512
201023120582,537
20111287284,407
2012219616 (4)4,930
20131390644,651
20142289244,695
20151712366,625
201612195108,470
201717240136,462
2018417746,574
201971611311,227
2020103271079,563
202113186110,414
2022142139 (5)13,393
20231434012 (4)10,916
2024724413 (1)47,210
20251122598 (1)34,506
2026526610 (2)—

What is it indicated for?

The TERUMOB SURSHIELDTMSAFETY WINGED BLOOD COLLECTION SET is a winged blood collection needle intended for venipuncture to collect blood specimens from patients. The TERUMOB SURSHIELDrM SAFETY WINGED BLOOD COLLECTION SET is also indicated for intravenous administration of fluids after removing the attached luer adapter from the blood collection set connector and attaching a syringe, or other coinpatible/appropriate device. This device may be used for any…

Read the full statement (115 words)

The TERUMOB SURSHIELDTMSAFETY WINGED BLOOD COLLECTION SET is a winged blood collection needle intended for venipuncture to collect blood specimens from patients.

The TERUMOB SURSHIELDrM SAFETY WINGED BLOOD COLLECTION SET is also indicated for intravenous administration of fluids after removing the attached luer adapter from the blood collection set connector and attaching a syringe, or other coinpatible/appropriate device. This device may be used for any patient population with consideration given to patient size, appropriateness for the solution being infused, and duration of therapy.

Additionally, after withdraw of the needle from the patient's vein, the attached needle safety shield can be manually activated to cover the needle immediately after USC to minimize risk of accidental needlestick.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K031279: Surshield Safety Winged Blood Collection Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K031279

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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