510(k) Report

510(k) · Cleared

Cleared

Versalet 7700 Care Center, Model # 7700

K993051510(k) TraditionalCleared Feb 3, 2000143-day reviewClass II21 CFR 880.5400

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

Hill-Rom Air-Shields · FMZ Incubator, Neonatal

Cleared on Feb 3, 2000 as substantially equivalent to K940951 (Air-Shields, Inc., 1995) and 3 other predicates after a 143-day review. Its family tree reaches back 3 generations to 1995. 1 of the 13 devices in its family, counting itself, has a Class I recall. 1 later device descends from it.

Decided
Feb 3, 2000
Review
143 days
Class
Class II
Product code
FMZ
Recalls
None
Predicates
4

Its longest line of descent runs back 3 generations to K942948 (1995). 11 ancestors in all, the oldest K912908 (1991). 1 later device descends from it, 1 citing it directly. 1 of the 13 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 1997: 1 other ancestor1996: 2 other ancestors1995: 3 other ancestors1994: 1 other ancestor, 1 with a Class I recall11991: 1 other ancestor2006: 1 descendant clearedK942948 · Stryker Powered Stretcher · Stryker Corp. · 1995K970074 · Stanilet Freestanding/CC Infant/2000C Infant Warmer (1250C/1500C/2000D) · Hill-Rom, Inc. · 1997K971366 · Incuwarmer · Hill-Rom, Inc. · 19981990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 5 other ancestors, 1 with a Class I recall1 1 generation forward: 1 descendant K971366 · Incuwarmer · Hill-Rom, Inc. · 1998K970074 · Stanilet Freestanding/CC Infant/2000C Infant Warmer (1250C/1500C/2000D) · Hill-Rom, Inc. · 1997K942948 · Stryker Powered Stretcher · Stryker Corp. · 19950
  1. Root · 3 generations backK942948 Stryker Powered StretcherStryker Corp. · 1995
  2. 2 generations backK970074 Stanilet Freestanding/CC Infant/2000C Infant Warmer…Hill-Rom, Inc. · 1997
  3. 1 generation backK971366 IncuwarmerHill-Rom, Inc. · 1998
  4. This deviceK993051 Versalet 7700 Care Center, Model # 7700Hill-Rom Air-Shields · 2000
  5. Descendant · cites it directly · 0 of its ownK053399 Versalet 7700 Care CenterDraeger Medical Infant Care, Inc. · 2006

Class I recalls in this family

Most influential descendants

Showing 1 of 1 · See all
  • K053399Versalet 7700 Care CenterDraeger Medical Infant Care, Inc. · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K942948Stryker Powered StretcherStryker Corp.1995—
−2K970074Stanilet Freestanding/CC Infant/2000C Infant Warmer (1250C/1500C/2000D)Hill-Rom, Inc.1997—
−1K971366IncuwarmerHill-Rom, Inc.1998—
0 (this device)K993051Versalet 7700 Care Center, Model # 7700Hill-Rom Air-Shields2000—
+1K053399Versalet 7700 Care CenterDraeger Medical Infant Care, Inc.2006—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199411
199530
199620
199710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K993051, 1995–2006Source: 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), 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.

1 device in this family has 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 FMZ device

  1. #1 K251663 Giraffe OmniBed Carestation (CS1); Giraffe…score 14.4 · 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? (4)

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
*K940951RW Resucitaire Infant Radiant Warmer
Summary page 1
…lds Resuscitaire® Radiant Warmer, Hill-Rom Air-Shields ISOLETTE® Infant Incubator, Hill-Rom Incuwarmer Driger Babytherm 8004 Babytherm 8010 September 09, 1999 (19505 K940951 K960980 K971366 K971198 Device Description The Versalet™ 7700 Care Center is a warming device that combines the…
Air-Shields, Inc.1995—
*K960980Isolette Infant Incubator
Summary page 1
…scitaire® Radiant Warmer, Hill-Rom Air-Shields ISOLETTE® Infant Incubator, Hill-Rom Incuwarmer Driger Babytherm 8004 Babytherm 8010 September 09, 1999 (19505 K940951 K960980 K971366 K971198 Device Description The Versalet™ 7700 Care Center is a warming device that combines the heating…
Air-Shields, Inc.1996—
*K971366Incuwarmer
Summary page 1
…® Radiant Warmer, Hill-Rom Air-Shields ISOLETTE® Infant Incubator, Hill-Rom Incuwarmer Driger Babytherm 8004 Babytherm 8010 September 09, 1999 (19505 K940951 K960980 K971366 K971198 Device Description The Versalet™ 7700 Care Center is a warming device that combines the heating technolo…
Hill-Rom, Inc.1998—
*K971198Babytherm 8004 Babytherm 8010
Summary page 1
…t Warmer, Hill-Rom Air-Shields ISOLETTE® Infant Incubator, Hill-Rom Incuwarmer Driger Babytherm 8004 Babytherm 8010 September 09, 1999 (19505 K940951 K960980 K971366 K971198 Device Description The Versalet™ 7700 Care Center is a warming device that combines the heating technologies of…
Drager, Inc.19971

Also cleared against K940951: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K053399Versalet 7700 Care CenterDraeger Medical Infant Care, Inc.20060

Has anything in its family been recalled? (1 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.

  • K943360Ohio Care Plus IncubatorOhmeda Medical · 1994 · 2 generations back · ◆ in the 1994 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 5 years and passes through 3 companies; a new generation was cleared every 2.1 years on median.
  • 3 of the 11 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K053399 (Draeger Medical Infant Care, Inc., 2006) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K940951.

How does its category compare?

All FMZ devices

FMZ Incubator, Neonatal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FMZ

2in 2025

2007: 32008: 12010: 42011: 12014: 12015: 12016: 12017: 12018: 22019: 22022: 12025: 22026 (partial year): 2
2007high 4 (2010) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMZ

60in 2010

2007: 81 days median2010: 60 days median
2007high 81 (2007) · low 60 (2010)2026

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

Recalls per year · FMZ

2in 2024

2008: 42011: 52013: 1, 1 Class I2016: 12018: 32019: 12023: 8, 8 Class I2024: 2, 2 Class I2026 (partial year): 3
2007high 8 (2023) · low 0 (2007)2026

Class I (11 since 2007) Class II/III not classified

Adverse event reports per year · FMZ

250in 2025

2007: 142008: 102009: 82010: 112011: 102012: 122013: 112014: 32015: 92016: 122017: 42018: 182019: 242020: 82021: 152022: 272023: 192024: 1182025: 250
2007high 250 (2025) · low 3 (2014)2025

MAUDE reports naming product code FMZ, 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
2007381014
20081—410
20090—08
2010460011
20111—510
20120—012
20130—1 (1)11
20141—03
20151—09
20161—112
20171—04
20182—318
20192—124
20200—08
20210—015
20221—027
20230—8 (8)19
20240—2 (2)118
20252—0250
20262—3—

What is it indicated for?

The Versalet 7700 Care Center is a mobile, caster mounted, neonatal device, which is used to assist in maintaining an infant’s skin temperature and thermal environment. The device accomplishes this using radiant and convective heat. Accessories and options to the device permit environmental control and monitoring including humidification. It is intended for in-patient use in maternity nurseries, and neonatal care environments of hospitals or other healthcare facilities.

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. “K993051: Versalet 7700 Care Center, Model # 7700.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K993051

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
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026