510(k) Report

510(k) · Cleared

Cleared

Isolette 8000 Plus

K182977510(k) SpecialCleared Nov 21, 201826-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

Draeger Medical Systems, Inc. · FMZ Incubator, Neonatal

Cleared on Nov 21, 2018 as substantially equivalent to K172154 (Draeger Medical Sytems, Inc., 2018) after a 26-day review. Its family tree reaches back 2 generations to 2000.

Decided
Nov 21, 2018
Review
26 days
Class
Class II
Product code
FMZ
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K001242 (2000). No later device cites it as a predicate yet.

  1. Root · 2 generations backK001242 Isolette Infant Incubator, Model C2HSHill-Rom Air-Shields · 2000
  2. 1 generation backK172154 Isolette 8000 plusDraeger Medical Sytems, Inc. · 2018
  3. This deviceK182977 Isolette 8000 PlusDraeger Medical Systems, Inc. · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K001242Isolette Infant Incubator, Model C2HSHill-Rom Air-Shields2000—
−1K172154Isolette 8000 plusDraeger Medical Sytems, Inc.2018—
0 (this device)K182977Isolette 8000 PlusDraeger Medical Systems, Inc.2018—
FIG. 1 — Lineage of K182977, 2000–2018Source: 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 FMZ? 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
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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
*K172154Isolette 8000 plus
Summary page 4
…Product Code: FMZ Class: II Predicate Device: Isolette® 8000 plus, K172154 Draeger Medical Systems, Inc. is submitting a special 510(k) premarket notification for a modification to an existing device, th…
Draeger Medical Sytems, Inc.2018—

Also cleared against K172154: 1 other device →

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 18 years and passes through 3 companies; a new generation was cleared every 17.8 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K172154.

How does its category compare?

All FMZ devices

FMZ Incubator, Neonatal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

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 Isolette® 8000 plus is indicated for thermoregulation and controlling oxygen (optional), and humidity (optional) for both premature and full-term infants up to a maximum of 10 kg (22lbs).

The Isolette® 8000 plus is not intended for home use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182977: Isolette 8000 Plus.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K182977

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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