510(k) Report

510(k) · Cleared

Cleared

Blood/Fluid Warmer Model DW-1000A

K770232510(k) TraditionalCleared Feb 14, 19777-day reviewClass II21 CFR 864.9205

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

Gorman Rupp Industries · BSB Warmer, Blood, Non-Electromagnetic Radiation

Cleared on Feb 14, 1977 after a 7-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 of the 19 devices in its family, counting itself, have a Class I recall. 18 later devices descend from it.

Decided
Feb 14, 1977
Review
7 days
Class
Class II
Product code
BSB
Recalls
None
Predicates
0

18 later devices descend from it, 3 citing it directly. 2 of the 19 devices in this family, counting this one, have a Class I recall.

Descendants, by year cleared 2001: 1 descendant cleared1996: 1 descendant cleared1999: 1 descendant cleared2011: 1 descendant cleared2006: 2 descendants cleared, 1 with a Class I recall12012: 3 descendants cleared2024: 1 descendant cleared2016: 1 descendant cleared2023: 1 descendant cleared2019: 2 descendants cleared2013: 1 descendant cleared, 1 with a Class I recall12017: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant cleared19801990200020102020
  1. This deviceK770232 Blood/Fluid Warmer Model DW-1000AGorman Rupp Industries · 1977
  2. Descendant · cites it directly · 16 of its ownK984640 Thermal AngelEstill Medical Technologies, Inc. · 1999 · Recalled
  3. Descendant · cites it directly · 13 of its ownK012031 Modification to Thermal AngelEstill Medical Technologies, Inc. · 2001 · Recalled
  4. Descendant · 2 generations on · 12 of its ownK060537 Eflow IV Fluid Warmer, Model 100, Eflow Disposable Cartridge, Model…Enginivity, LLC · 2006 · Recalled (Class I)
  5. Descendant · 3 generations on · 10 of its ownK112902 Enflow IV Fluid WarmerVital Signs, Inc. · 2012
  6. Descendant · 4 generations on · 1 of its ownK232107 °M Warmer SystemMequ A/S · 2024

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

1996: 11999: 12001: 12006: 22011: 12012: 32013: 12016: 12017: 12019: 22023: 12024: 12025: 12026: 1
1996high 3 (2012) · low 0 (1997)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 18 · See all
  • K984640Thermal AngelEstill Medical Technologies, Inc. · 1999 · cites it directly16descendants
  • K012031Modification to Thermal AngelEstill Medical Technologies, Inc. · 2001 · cites it directly13descendants
  • K060537Eflow IV Fluid Warmer, Model 100, Eflow Disposable Cartridge, Model 200 and Eflow AC…Enginivity, LLC · 2006 · 2 generations on12descendants
  • K112902Enflow IV Fluid WarmerVital Signs, Inc. · 2012 · 3 generations on10descendants
  • K232107°M Warmer SystemMequ A/S · 2024 · 4 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K770232Blood/Fluid Warmer Model DW-1000AGorman Rupp Industries1977—
+1K984640Thermal AngelEstill Medical Technologies, Inc.19991
+1K012031Modification to Thermal AngelEstill Medical Technologies, Inc.20011
+2K060537Eflow IV Fluid Warmer, Model 100, Eflow Disposable Cartridge, Model 200 and…Enginivity, LLC2006Class I
+3K112902Enflow IV Fluid WarmerVital Signs, Inc.2012—
+4K232107°M Warmer SystemMequ A/S2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199910
200110
200621
201110
201230
201311
201610
201710
201920
202310
202410
202510
202610
FIG. 1 — Lineage of K770232, 1977–2026Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

2 devices in this family have a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (18)

See all 18

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

NumberDeviceApplicantDecidedDescendants
K984640Thermal AngelEstill Medical Technologies, Inc.199916
K012031Modification to Thermal AngelEstill Medical Technologies, Inc.200113
K953741Thermacyl Blood/Fluid WarmerBaxter Healthcare Corp19960

Has anything in its family been recalled? (2 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.

  • K060537Eflow IV Fluid Warmer, Model 100, Eflow Disposable Cartridge, Model 200 and Eflow AC Power Supply, Model 120Enginivity, LLC · 2006 · 2 generations on · ◆ in the 2006 descendants bar of FIG. 12 Class I recalls
  • K130867Enflow IV Fluid Warmer Insulated StrapVital Signs, Inc., A GE Healthcare Company · 2013 · 5 generations on · ◆ in the 2013 descendants bar of FIG. 12 Class I recalls

What does this lineage say?

  • Of its descendants, K984640 (Estill Medical Technologies, Inc., 1999) has gone furthest, with 16 descendants of its own.

How does its category compare?

All BSB devices

BSB Warmer, Blood, Non-Electromagnetic Radiation: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · BSB

1in 2011

2009: 12011: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BSB

Too few BSB 510(k)s in any year since 2007 to give a median.

Recalls per year · BSB

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

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

Adverse event reports per year · BSB

197in 2025

2007: 42008: 52010: 62011: 352012: 42013: 52014: 102015: 112016: 662017: 292018: 362019: 1472020: 2162021: 3402022: 4472023: 2902024: 2822025: 197
2007high 447 (2022) · low 0 (2009)2025

MAUDE reports naming product code BSB, 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
20070—04
20080—05
20091—00
20100—06
20111—035
20120—04
20130—05
20140—110
20150—011
20160—066
20170—029
20180—036
20190—0147
20200—0216
20210—0340
20220—0447
20230—0290
20240—0282
20250—0197
20260—0—
Cite this page

510(k) Report. “K770232: Blood/Fluid Warmer Model DW-1000A.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K770232

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026