510(k) Report

510(k) · Cleared

Cleared

Phototherapy Unit 7850 Neonatal Photo

K840454510(k) TraditionalCleared Mar 23, 198460-day reviewClass II21 CFR 880.5700

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

Air-Shields, Inc. · LBI Unit, Neonatal Phototherapy

Cleared on Mar 23, 1984 after a 60-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Mar 23, 1984
Review
60 days
Class
Class II
Product code
LBI
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared19801990200020102020
  1. This deviceK840454 Phototherapy Unit 7850 Neonatal PhotoAir-Shields, Inc. · 1984
  2. Descendant · cites it directly · 0 of its ownK021531 Rpi Replacement Phototherapy LightsReplacement Parts Industries, Inc. · 2002

Most influential descendants

Showing 1 of 1 · See all
  • K021531Rpi Replacement Phototherapy LightsReplacement Parts Industries, Inc. · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K840454Phototherapy Unit 7850 Neonatal PhotoAir-Shields, Inc.1984—
+1K021531Rpi Replacement Phototherapy LightsReplacement Parts Industries, Inc.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K840454, 1984–2002Source: 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.

Planning a device in LBI? 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 LBI device

  1. #1 K251308 SnugLit (TM) Wearable Phototherapy System…score 11.6 · 4 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K021531Rpi Replacement Phototherapy LightsReplacement Parts Industries, Inc.20020

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, K021531 (Replacement Parts Industries, Inc., 2002) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LBI devices

LBI Unit, Neonatal Phototherapy: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LBI

1in 2025

2007: 32009: 22010: 12011: 32012: 52014: 12015: 12016: 32017: 22018: 22019: 12020: 12021: 12025: 12026 (partial year): 1
2007high 5 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LBI

134in 2016

2007: 91 days median2011: 157 days median2012: 108 days median2016: 134 days median
2007high 157 (2011) · low 91 (2007)2026

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

Recalls per year · LBI

1in 2019

2009: 12014: 12015: 12016: 22019: 1
2007high 2 (2016) · low 0 (2007)2026

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

Adverse event reports per year · LBI

3in 2025

2007: 12008: 42009: 42010: 92011: 52012: 32013: 62014: 52015: 62016: 222017: 5772018: 372019: 62020: 62021: 22022: 82024: 62025: 3
2007high 577 (2017) · low 0 (2023)2025

MAUDE reports naming product code LBI, 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
200739101
20080—04
20092—14
20101—09
2011315705
2012510803
20130—06
20141—15
20151—16
20163134222
20172—0577
20182—037
20191—16
20201—06
20211—02
20220—08
20230—00
20240—06
20251—03
20261—0—
Cite this page

510(k) Report. “K840454: Phototherapy Unit 7850 Neonatal Photo.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K840454

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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