510(k) Report

FDA product code · General and plastic surgery

Light Based Imaging

PSNClass II21 CFR 878.4580510(k) required10 decisions since 20020 recalls

10 FDA decisions since 2002. 510(k) reviews decided 2021–2025 took a median of 85 days (half between 85 and 176). No recall names this code. The most-cited predicate is K023729, named by 2 later devices.

Emission and collection of light to create an image for medical purposes

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

FIG. A — Illustration, general and plastic surgery panel

Twenty years of PSN at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · PSN

1in 2023

2007: 12008: 12018: 12019: 12021: 12022: 12023: 1
2007high 1 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PSN

Too few PSN 510(k)s in any year since 2007 to give a median.

Recalls per year · PSN

No recall names PSN since 2007.

Adverse event reports per year · PSN

No MAUDE report names PSN since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—00
20081—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—00
20191—00
20200—00
20211—00
20221—00
20231—00
20240—00
20250—00
20260—0—
FIG. 1 — PSN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in PSN? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 878.4580.