510(k) Report

FDA product code · Radiology

Device, Digital Image Storage, Radiological

LMBClass I21 CFR 892.2010510(k) exempt55 decisions since 198313 recalls

FDA lists LMB as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 892.9 applies, such as a new intended use or a different fundamental technology. 55 FDA decisions since 1983. 13 recalls name this code, 0 of them Class I. The most-cited predicate is K955237, named by 6 later devices.

Medical image storage hardware is a device that provides electronic maintenance and access functions for medical images.

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, radiology panel

Twenty years of LMB 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 · LMB

FDA has decided no LMB device since 2007.

Median 510(k) review, days · LMB

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

Recalls per year · LMB

1in 2013

2008: 12009: 52011: 22013: 1
2007high 5 (2009) · low 0 (2007)2026

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

Adverse event reports per year · LMB

7in 2025

2007: 12008: 32009: 32010: 162011: 42012: 42013: 72014: 12016: 212017: 102018: 52019: 102020: 82021: 102023: 102024: 92025: 7
2007high 21 (2016) · low 0 (2015)2025

MAUDE reports naming product code LMB, 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—01
20080—13
20090—53
20100—016
20110—24
20120—04
20130—17
20140—01
20150—00
20160—021
20170—010
20180—05
20190—010
20200—08
20210—010
20220—00
20230—010
20240—09
20250—07
20260—0—
FIG. 1 — LMB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LMB? 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 892.2010.