510(k) Report

510(k) · Cleared

Cleared

S-Line

K213191510(k) TraditionalCleared May 24, 2022237-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

Barkey GmbH & Co. KG · LGZ Warmer, Thermal, Infusion Fluid

Cleared on May 24, 2022 as substantially equivalent to K121198 (Biegler GmbH, 2012) after a 237-day review. Its family tree reaches back 2 generations to 1996.

Decided
May 24, 2022
Review
237 days
Class
Class II
Product code
LGZ
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K954769 (1996). No later device cites it as a predicate yet.

  1. Root · 2 generations backK954769 Biegler BW385L Blood & Infusion WarmerBiegler Medical Products, Inc. · 1996
  2. 1 generation backK121198 BW685, BW685SBiegler GmbH · 2012
  3. This deviceK213191 S-LineBarkey GmbH & Co. KG · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K954769Biegler BW385L Blood & Infusion WarmerBiegler Medical Products, Inc.1996—
−1K121198BW685, BW685SBiegler GmbH2012—
0 (this device)K213191S-LineBarkey GmbH & Co. KG2022—
FIG. 1 — Lineage of K213191, 1996–2022Source: 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 LGZ? 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 LGZ device

  1. #1 K260988 °M Warmer System with °M Stationscore 12.7 · 6 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
*K121198BW685, BW685S
Summary page 4
…, Thermal, Infusion Fluid Product Classification: LGZ CFR: Unclassified Predicate Device: K121198 Tradename: Biegler BW685S Classification Name: Warmer, Thermal, Infusion Flui…
Biegler GmbH2012—

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?

  • The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 15.9 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All LGZ devices

LGZ Warmer, Thermal, Infusion Fluid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · LGZ

2in 2025

2007: 22008: 42009: 22010: 22011: 32012: 72013: 52015: 22016: 22017: 22018: 12019: 32022: 32023: 12024: 12025: 22026 (partial year): 2
2007high 7 (2012) · low 0 (2014)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LGZ

546in 2022

2008: 99 days median2011: 77 days median2012: 162 days median2013: 143 days median2019: 209 days median2022: 546 days median
2007high 546 (2022) · low 77 (2011)2026

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

Recalls per year · LGZ

1in 2016

2009: 12010: 12011: 82015: 12016: 12026 (partial year): 1
2007high 8 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LGZ

376in 2025

2007: 112008: 102009: 122010: 432011: 542012: 522013: 162014: 232015: 342016: 152017: 582018: 942019: 3402020: 1,2212021: 8852022: 1,5482023: 1,0332024: 8622025: 376
2007high 1,548 (2022) · low 10 (2008)2025

MAUDE reports naming product code LGZ, 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
20072—011
2008499010
20092—112
20102—143
2011377854
20127162052
20135143016
20140—023
20152—134
20162—115
20172—058
20181—094
201932090340
20200—01,221
20210—0885
2022354601,548
20231—01,033
20241—0862
20252—0376
20262—1—

What is it indicated for?

The Barkey S-Line blood / fluid warming system is intended to deliver warm blood, blood products, and liquids to adult and pediatric patients. It delivers the fluid via intravenous (IV) administration in hospitals and clinical settings where warmed intravenous fluids are required.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K213191: S-Line.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213191

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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