510(k) Report

510(k) · Cleared

Cleared

Ferno Washington Incubator Transporter, Mod. 35-IT

K932417510(k) TraditionalCleared Sep 9, 1993114-day reviewClass II21 CFR 880.5410

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

Ferno-Washington, Inc. · FPL Incubator, Neonatal Transport

Cleared on Sep 9, 1993 after a 114-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Sep 9, 1993
Review
114 days
Class
Class II
Product code
FPL
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K932417Source: FDA 510(k) database · 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 FPL? 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 FPL device

  1. #1 K220742 NxtGen Infant Transport Incubatorscore 4.3 · 3 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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.

How does its category compare?

All FPL devices

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

FDA decisions per year · FPL

1in 2022

2008: 12011: 42013: 12014: 12017: 12022: 1
2007high 4 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FPL

148in 2011

2011: 148 days median
2007high 148 (2011)2026

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

Recalls per year · FPL

No recall names FPL since 2007.

Adverse event reports per year · FPL

3in 2024

2010: 42011: 12013: 32014: 12015: 12016: 12018: 22020: 12021: 22022: 12024: 3
2007high 4 (2010) · low 0 (2007)2025

MAUDE reports naming product code FPL, 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—00
20081—00
20090—00
20100—04
2011414801
20120—00
20131—03
20141—01
20150—01
20160—01
20171—00
20180—02
20190—00
20200—01
20210—02
20221—01
20230—00
20240—03
20250—00
20260—0—
Cite this page

510(k) Report. “K932417: Ferno Washington Incubator Transporter, Mod. 35-IT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K932417

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
  • Page last updated Nov 3, 2026