510(k) · Cleared
ClearedBD Vacutainer Safety-Lok Administration Set with Filter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Becton, Dickinson & CO · FPA Set, Administration, Intravascular
Cleared on Nov 18, 2003 as substantially equivalent to K980414 (Bd Becton Dickinson Vacutainer Systems Preanalytic, 1998) after a 29-day review. Its family tree reaches back 2 generations to 1997. 5 later devices descend from it.
- Decided
- Nov 18, 2003
- Review
- 29 days
- Class
- Class II
- Product code
- FPA
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K970259 (1997). 5 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK970259 E-Z Set Infusion Set/Saf-T E-Z Set Infusion SetBecton Dickinson Vascular Access, Inc. · 1997
- 1 generation backK980414 Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple…Bd Becton Dickinson Vacutainer Systems Preanalytic · 1998 · Recalled
- This deviceK033350 BD Vacutainer Safety-Lok Administration Set with FilterBecton, Dickinson & CO · 2003
- Descendant · cites it directly · 4 of its ownK070547 Surflo Winged Infusion Set with Filter and Needle Protection…Terumo Europe N.V. · 2007
- Descendant · 2 generations on · 2 of its ownK100946 Intravscular Administration SetTerumo Europe N.V. · 2010
- Descendant · 2 generations on · 0 of its ownK140175 Intravascular Administration SetDelta Med Spa · 2014
- Descendant · 2 generations on · 0 of its ownK133894 Surflo Winged Infusion Set with Filter & Needle Protection (Surshield)Terumo Europe N.V. · 2014 · Recalled
- Descendant · 3 generations on · 0 of its ownK133867 Surflo Winged Infusion Set with Needle Protection (Surshield)Terumo Europe N.V. · 2014
Most influential descendants
Showing 5 of 5 · See all- K070547Surflo Winged Infusion Set with Filter and Needle Protection (Surshield)Terumo Europe N.V. · 2007 · cites it directly4descendants
- K100946Intravscular Administration SetTerumo Europe N.V. · 2010 · 2 generations on2descendants
- K140175Intravascular Administration SetDelta Med Spa · 2014 · 2 generations on0descendants
- K133894Surflo Winged Infusion Set with Filter & Needle Protection (Surshield)Terumo Europe N.V. · 2014 · 2 generations on0descendants
- K133867Surflo Winged Infusion Set with Needle Protection (Surshield)Terumo Europe N.V. · 2014 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K970259 | E-Z Set Infusion Set/Saf-T E-Z Set Infusion Set | Becton Dickinson Vascular Access, Inc. | 1997 | — |
| −1 | K980414 | Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple, Vacutainer… | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1998 | 1 |
| 0 (this device) | K033350 | BD Vacutainer Safety-Lok Administration Set with Filter | Becton, Dickinson & CO | 2003 | — |
| +1 | K070547 | Surflo Winged Infusion Set with Filter and Needle Protection (Surshield) | Terumo Europe N.V. | 2007 | — |
| +2 | K100946 | Intravscular Administration Set | Terumo Europe N.V. | 2010 | — |
| +2 | K140175 | Intravascular Administration Set | Delta Med Spa | 2014 | — |
| +2 | K133894 | Surflo Winged Infusion Set with Filter & Needle Protection (Surshield) | Terumo Europe N.V. | 2014 | 1 |
| +3 | K133867 | Surflo Winged Infusion Set with Needle Protection (Surshield) | Terumo Europe N.V. | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 1 | 0 |
| 2010 | 1 | 0 |
| 2014 | 3 | 0 |
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 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
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 | Decided |
|---|---|---|---|
| * | K980414 | Vacutainer Brand Safety-Lok Blood Collection Set Model Multiple, Vacutainer Brand Blood…Summary page 2…ed in the table below. Manufacturer Predicate Device K-Number Clearance Date Becton BD Vacutainea K980414 March 3, 1998 Dickinson Safety-LokTMBlood Collection Set Re… | 1998 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K070547 | Surflo Winged Infusion Set with Filter and Needle Protection (Surshield) | 2007 | 4 |
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 3 companies; a new generation was cleared every 5.7 years on median.
- 1 of the 2 ancestors has a recall of any class.
- Of its descendants, K070547 (Terumo Europe N.V., 2007) has gone furthest, with 4 descendants of its own.
- 11 other devices also cite its predicate K980414.
How does its category compare?
All FPA devicesFPA Set, Administration, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FPA
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FPA
225in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FPA
98in 2025
Class I (17 since 2007) Class II/III not classified
Adverse event reports per year · FPA
34,506in 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 BD Vacutainer Safety-Lok Administration Set with Filter is a sterile, single-use wing set intended for the intravenous administration of fluids and may be used for any patient population with consideration given to patient size, appropriateness for the solution being infused and duration of therapy. The BD Vacutainer Safety-Lok Administration Set with Filter minimizes the possibility of needlesticks if manually activated following administration.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K033350 · printed Nov 6, 2026
Cite this page
510(k) Report. “K033350: BD Vacutainer Safety-Lok Administration Set with Filter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K033350
Report an extraction error
Are you the manufacturer?
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