510(k) Report

510(k) · Cleared

Cleared

Atom Infa Warmer V-505

K002355510(k) AbbreviatedCleared Oct 10, 200069-day reviewClass II21 CFR 880.5130

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

Atom Medical Corp · FMT Warmer, Infant Radiant

Cleared on Oct 10, 2000 after a 69-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 of the 20 devices in its family, counting itself, have a Class I recall. 19 later devices descend from it.

Decided
Oct 10, 2000
Review
69 days
Class
Class II
Product code
FMT
Recalls
None
Predicates
0

19 later devices descend from it, 5 citing it directly. 6 of the 20 devices in this family, counting this one, have a Class I recall.

Descendants, by year cleared 2007: 4 descendants cleared, 3 with a Class I recall32006: 2 descendants cleared2011: 4 descendants cleared2010: 3 descendants cleared, 1 with a Class I recall12014: 2 descendants cleared2013: 1 descendant cleared, 1 with a Class I recall12009: 1 descendant cleared, 1 with a Class I recall12018: 1 descendant cleared2019: 1 descendant cleared200020052010201520202025
  1. This deviceK002355 Atom Infa Warmer V-505Atom Medical Corp · 2000
  2. Descendant · cites it directly · 10 of its ownK070210 Giraffe and Panda T- Piece Resuscitation SystemOhmeda Medical · 2007 · Recalled (Class I)
  3. Descendant · cites it directly · 4 of its ownK070247 Giraffe and Panda Bag and Mask Resuscitation SystemOhmeda Medical · 2007 · Recalled (Class I)
  4. Descendant · cites it directly · 4 of its ownK061856 V-2200 Infant IncubatorAtom Medical, Inc. · 2006
  5. Descendant · cites it directly · 3 of its ownK070377 Giraffe and Panda WarmerOhmeda Medical · 2007 · Recalled (Class I)
  6. Descendant · 2 generations on · 2 of its ownK072157 Modification to Giraffe and Panda Warmers (Giraffe and Panda…Ohmeda Medical · 2007 · Recalled

Showing 5 of 19 descendants. See all descendants

Descendants cleared per year

2006: 22007: 42009: 12010: 32011: 42013: 12014: 22018: 12019: 1
2006high 4 (2007) · low 0 (2008)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 19 · See all
  • K070210Giraffe and Panda T- Piece Resuscitation SystemOhmeda Medical · 2007 · cites it directly10descendants
  • K070247Giraffe and Panda Bag and Mask Resuscitation SystemOhmeda Medical · 2007 · cites it directly4descendants
  • K061856V-2200 Infant IncubatorAtom Medical, Inc. · 2006 · cites it directly4descendants
  • K070377Giraffe and Panda WarmerOhmeda Medical · 2007 · cites it directly3descendants
  • K072157Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible Power Supply)Ohmeda Medical · 2007 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002355Atom Infa Warmer V-505Atom Medical Corp2000—
+1K070210Giraffe and Panda T- Piece Resuscitation SystemOhmeda Medical2007Class I
+1K070247Giraffe and Panda Bag and Mask Resuscitation SystemOhmeda Medical2007Class I
+1K061856V-2200 Infant IncubatorAtom Medical, Inc.2006—
+1K070377Giraffe and Panda WarmerOhmeda Medical2007Class I
+2K072157Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible…Ohmeda Medical20071

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200620
200743
200911
201031
201140
201311
201420
201810
201910
FIG. 1 — Lineage of K002355, 2000–2019Source: 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.

6 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.

Top candidate predicates for a new FMT device

  1. #1 K243606 Babyroo TN300score 9.3 · 3 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?

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

What descends from it? (19)

See all 19

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

NumberDeviceApplicantDecidedDescendants
K070210Giraffe and Panda T- Piece Resuscitation System Class IOhmeda Medical200710
K070247Giraffe and Panda Bag and Mask Resuscitation System Class IOhmeda Medical20074
K061856V-2200 Infant IncubatorAtom Medical, Inc.20064
K070377Giraffe and Panda Warmer Class IOhmeda Medical20073
K060461V-505 Infa WarmerAtom Medical, Inc.20062

Has anything in its family been recalled? (6 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.

  • K070377Giraffe and Panda WarmerOhmeda Medical · 2007 · Cites it directly · ◆ in the 2007 descendants bar of FIG. 11 Class I recall
  • K070247Giraffe and Panda Bag and Mask Resuscitation SystemOhmeda Medical · 2007 · Cites it directly · ◆ in the 2007 descendants bar of FIG. 13 Class I recalls
  • K070210Giraffe and Panda T- Piece Resuscitation SystemOhmeda Medical · 2007 · Cites it directly · ◆ in the 2007 descendants bar of FIG. 13 Class I recalls
  • K093913Mercury Medical T-Piece ResuscitatorMercury Medical, Inc. · 2010 · 2 generations on · ◆ in the 2010 descendants bar of FIG. 12 Class I recalls
  • K123309Giraffe and Panda WarmersOhmeda Medical · 2013 · 2 generations on · ◆ in the 2013 descendants bar of FIG. 13 Class I recalls
  • K090697Modification to: Giraffe and Panda WarmerOhmeda Medical · 2009 · 2 generations on · ◆ in the 2009 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • Of its descendants, K070210 (Ohmeda Medical, 2007) has gone furthest, with 10 descendants of its own.

How does its category compare?

All FMT devices

FMT Warmer, Infant Radiant: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FMT

1in 2025

2007: 22009: 12010: 12011: 12012: 42013: 12018: 12020: 22021: 12022: 12023: 12025: 1
2007high 4 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMT

103in 2012

2012: 103 days median
2007high 103 (2012)2026

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

Recalls per year · FMT

4in 2019

2008: 12009: 22013: 22014: 12015: 12016: 12018: 42019: 4, 4 Class I2026 (partial year): 2, 2 Class I
2007high 4 (2018) · low 0 (2007)2026

Class I (6 since 2007) Class II/III not classified

Adverse event reports per year · FMT

359in 2025

2007: 212008: 1142009: 802010: 1062011: 792012: 542013: 552014: 792015: 562016: 562017: 462018: 792019: 1,4372020: 1,6052021: 4732022: 1532023: 1752024: 2572025: 359
2007high 1,605 (2020) · low 21 (2007)2025

MAUDE reports naming product code FMT, 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—021
20080—1114
20091—280
20101—0106
20111—079
20124103054
20131—255
20140—179
20150—156
20160—156
20170—046
20181—479
20190—4 (4)1,437
20202—01,605
20211—0473
20221—0153
20231—0175
20240—0257
20251—0359
20260—2 (2)—
Cite this page

510(k) Report. “K002355: Atom Infa Warmer V-505.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K002355

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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