510(k) Report

510(k) · Cleared

Cleared

Temp Marq (TM) Convective Warming System

K904690510(k) TraditionalCleared Feb 1, 1991108-day reviewClass II21 CFR 870.5900

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

Marquest Medical Products, Inc. · DWJ System, Thermal Regulating

Cleared on Feb 1, 1991 after a 108-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 10 later devices descend from it.

Decided
Feb 1, 1991
Review
108 days
Class
Class II
Product code
DWJ
Recalls
None
Predicates
0

10 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2001: 1 descendant cleared1997: 1 descendant cleared2009: 1 descendant cleared2014: 1 descendant cleared2006: 1 descendant cleared2012: 2 descendants cleared2010: 1 descendant cleared2013: 1 descendant cleared2018: 1 descendant cleared1990200020102020
  1. This deviceK904690 Temp Marq (TM) Convective Warming SystemMarquest Medical Products, Inc. · 1991
  2. Descendant · cites it directly · 8 of its ownK011907 Snuggle Warm 4000 Convective Warming SystemSims Level 1, Inc. · 2001 · Recalled
  3. Descendant · 2 generations on · 3 of its ownK061513 Level 1 Snuggle Warm Pediatric and Large Pediatric Underbody BlanketSmiths Medical Asd, Inc. · 2006
  4. Descendant · 2 generations on · 2 of its ownK101148 Warm Air Model 135 Hyperthermia System and BlanketsCincinnati Sub-Zero Products, Inc. · 2010 · Recalled
  5. Descendant · 2 generations on · 2 of its ownK083336 Level 1 Snuggle Warm Adult Underbody Convective Warming Blanket…Smiths Medical Asd, Inc. · 2009
  6. Descendant · 2 generations on · 1 of its ownK141686 Equator Convective Warmer, Snuggle Warm Adult Full Body Convective…Smith Medical Asd, Inc. · 2014

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

1997: 12001: 12006: 12009: 12010: 12012: 22013: 12014: 12018: 1
1997high 2 (2012) · low 0 (1998)2026

Most influential descendants

Showing 5 of 10 · See all
  • K011907Snuggle Warm 4000 Convective Warming SystemSims Level 1, Inc. · 2001 · cites it directly8descendants
  • K061513Level 1 Snuggle Warm Pediatric and Large Pediatric Underbody BlanketSmiths Medical Asd, Inc. · 2006 · 2 generations on3descendants
  • K101148Warm Air Model 135 Hyperthermia System and BlanketsCincinnati Sub-Zero Products, Inc. · 2010 · 2 generations on2descendants
  • K083336Level 1 Snuggle Warm Adult Underbody Convective Warming Blanket, Model SW-2013, Level 1…Smiths Medical Asd, Inc. · 2009 · 2 generations on2descendants
  • K141686Equator Convective Warmer, Snuggle Warm Adult Full Body Convective Warming Blanket…Smith Medical Asd, Inc. · 2014 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K904690Temp Marq (TM) Convective Warming SystemMarquest Medical Products, Inc.1991—
+1K011907Snuggle Warm 4000 Convective Warming SystemSims Level 1, Inc.20011
+2K061513Level 1 Snuggle Warm Pediatric and Large Pediatric Underbody BlanketSmiths Medical Asd, Inc.2006—
+2K101148Warm Air Model 135 Hyperthermia System and BlanketsCincinnati Sub-Zero Products, Inc.20102
+2K083336Level 1 Snuggle Warm Adult Underbody Convective Warming Blanket, Model…Smiths Medical Asd, Inc.2009—
+2K141686Equator Convective Warmer, Snuggle Warm Adult Full Body Convective Warming…Smith Medical Asd, Inc.2014—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
200110
200610
200910
201010
201220
201310
201410
201810
FIG. 1 — Lineage of K904690, 1991–2018Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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.

Planning a device in DWJ? 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 DWJ device

  1. #1 K260278 ThermAffyx (TM) Patient Safety Systemscore 12.8 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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? (10)

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

NumberDeviceApplicantDecidedDescendants
K011907Snuggle Warm 4000 Convective Warming SystemSims Level 1, Inc.20018
K963731Tru-5000 Thermal Recovery Radiant Heating UnitEnthermics Medical Systems, Inc.19970

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?

  • Of its descendants, K011907 (Sims Level 1, Inc., 2001) has gone furthest, with 8 descendants of its own.

How does its category compare?

All DWJ devices

DWJ System, Thermal Regulating: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DWJ

3in 2025

2007: 42008: 32009: 32010: 82011: 42012: 52013: 52014: 42016: 22017: 52018: 32019: 22020: 52021: 22022: 22023: 62024: 22025: 32026 (partial year): 5
2007high 8 (2010) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DWJ

131in 2025

2007: 106 days median2008: 73 days median2009: 106 days median2010: 134 days median2011: 180 days median2012: 69 days median2013: 77 days median2014: 131 days median2017: 153 days median2018: 95 days median2020: 30 days median2023: 42 days median2025: 131 days median2026 (partial year): 99 days median
2007high 180 (2011) · low 30 (2020)2026

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

Recalls per year · DWJ

3in 2024

2009: 62010: 22011: 72012: 12013: 22015: 12017: 32018: 52019: 32020: 22021: 12022: 52024: 32026 (partial year): 3
2007high 7 (2011) · low 0 (2007)2026

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

Adverse event reports per year · DWJ

2,384in 2025

2007: 522008: 402009: 712010: 1042011: 1362012: 1062013: 732014: 1162015: 2452016: 1,4002017: 1,4732018: 1,5172019: 2,2942020: 2,5462021: 2,6892022: 3,2262023: 3,4552024: 3,3292025: 2,384
2007high 3,455 (2023) · low 40 (2008)2025

MAUDE reports naming product code DWJ, 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
20074106052
2008373040
20093106671
201081342104
201141807136
20125691106
2013577273
201441310116
20150—1245
20162—01,400
2017515331,473
201839551,517
20192—32,294
202053022,546
20212—12,689
20222—53,226
202364203,455
20242—33,329
2025313102,384
20265993—
Cite this page

510(k) Report. “K904690: Temp Marq (TM) Convective Warming System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K904690

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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