510(k) Report

510(k) · Cleared

Cleared

Concert Medical Hands-Free Syringe (HFS)

K153599510(k) TraditionalCleared Sep 1, 2016260-day reviewClass II21 CFR 880.5725

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

Concert Medical, LLC · FRN Pump, Infusion

Cleared on Sep 1, 2016 as substantially equivalent to K980738 (Byron Medical, 1998) after a 260-day review. Its family tree reaches back 3 generations to 1980. 1 later device descends from it.

Decided
Sep 1, 2016
Review
260 days
Class
Class II
Product code
FRN
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K800560 (1980). 7 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors3 generations back: 2 other ancestors 1 generation forward: 1 descendant K980738 · Psi-Tec Syringe Infusion Pump and Accessories for General Fluid Irrigaion/Infiltration · Byron Medical · 1998K973133 · Big Bag 3000 Pressure Infusor · Byron Medical · 1997K800560 · MX820-5 Pressure Infusor 500CC MX820-10 · Medex, Inc. · 19800
  1. Root · 3 generations backK800560 MX820-5 Pressure Infusor 500CC MX820-10Medex, Inc. · 1980
  2. 2 generations backK973133 Big Bag 3000 Pressure InfusorByron Medical · 1997
  3. 1 generation backK980738 Psi-Tec Syringe Infusion Pump and Accessories for General Fluid…Byron Medical · 1998
  4. This deviceK153599 Concert Medical Hands-Free Syringe (HFS)Concert Medical, LLC · 2016
  5. Descendant · cites it directly · 0 of its ownK230083 SafiraMedovate Limited · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K230083SafiraMedovate Limited · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K800560MX820-5 Pressure Infusor 500CC MX820-10Medex, Inc.1980—
−2K973133Big Bag 3000 Pressure InfusorByron Medical1997—
−1K980738Psi-Tec Syringe Infusion Pump and Accessories for General Fluid…Byron Medical1998—
0 (this device)K153599Concert Medical Hands-Free Syringe (HFS)Concert Medical, LLC2016—
+1K230083SafiraMedovate Limited2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198220
199310
199510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K153599, 1980–2023Source: 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 FRN? 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 FRN device

  1. #1 K253703 RemunityPRO+ Pump for Remodulin®…score 12.6 · 4 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
*K980738Psi-Tec Syringe Infusion Pump and Accessories for General Fluid Irrigaion/Infiltration
Summary page 4
…25; Class 11 Psi-Tec Syringe Infusion Pump and Accessories Psi-Tec Syringe Infusion Pump and Accessories Infusion Pump FRN Infusion Pump 21 CFR 880.5725; Class 11 K980738; Byron Medical Psi-Tec Syringe Infusion Pump and Accessories SE date June 16, 1998 KleinTouch Pump KleinTouch Pump Infusion P…
Byron Medical1998—
†K123822Klein Touch Pump and Disposable Tubing SetHk Surgical, Inc.2013—
†K031128B-Smart, Model B-01Macosta Medical USA, LLC2004—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K230083SafiraMedovate Limited20230

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 36 years and passes through 3 companies; a new generation was cleared every 17.4 years on median.
  • None of the 7 ancestors has a recall.
  • Of its descendants, K230083 (Medovate Limited, 2023) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FRN devices

FRN Pump, Infusion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · FRN

8in 2025

2007: 122008: 82009: 92010: 32011: 32012: 42013: 62014: 62015: 32016: 32017: 32018: 32019: 22020: 12021: 22022: 62023: 72024: 52025: 82026 (partial year): 2
2007high 12 (2007) · low 1 (2020)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRN

172in 2025

2007: 102 days median2008: 89 days median2009: 66 days median2010: 93 days median2011: 103 days median2012: 217 days median2013: 312 days median2014: 172 days median2015: 232 days median2016: 301 days median2017: 305 days median2018: 267 days median2022: 268 days median2023: 265 days median2024: 103 days median2025: 172 days median
2007high 312 (2013) · low 66 (2009)2026

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

Recalls per year · FRN

7in 2025

2007: 152008: 242009: 1022010: 372011: 692012: 42, 2 Class I2013: 22, 3 Class I2014: 4, 3 Class I2015: 52016: 7, 1 Class I2017: 132018: 12019: 18, 1 Class I2020: 16, 5 Class I2021: 3, 2 Class I2022: 22023: 16, 10 Class I2024: 9, 4 Class I2025: 7, 4 Class I2026 (partial year): 11, 2 Class I
2007high 102 (2009) · low 1 (2018)2026

Class I (37 since 2007) Class II/III not classified

Adverse event reports per year · FRN

52,792in 2025

2007: 1,0862008: 8,2612009: 1,9522010: 6,1332011: 41,3672012: 15,4822013: 40,0822014: 94,1802015: 26,7422016: 16,5602017: 12,0602018: 16,5912019: 15,8502020: 94,1862021: 199,3422022: 888,0202023: 165,8382024: 57,7302025: 52,792
2007high 888,020 (2022) · low 1,086 (2007)2025

MAUDE reports naming product code FRN, 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
200712102151,086
2008889248,261
20099661021,952
2010393376,133
201131036941,367
2012421742 (2)15,482
2013631222 (3)40,082
201461724 (3)94,180
20153232526,742
201633017 (1)16,560
201733051312,060
20183267116,591
20192—18 (1)15,850
20201—16 (5)94,186
20212—3 (2)199,342
202262682888,020
2023726516 (10)165,838
202451039 (4)57,730
202581727 (4)52,792
20262—11 (2)—

What is it indicated for?

The Concert Medical Hands-Free Syringe (HFS) is indicated for general fluid irrigation/infiltration.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K153599: Concert Medical Hands-Free Syringe (HFS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K153599

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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