510(k) Report

FDA product code · General hospital

Manometer, Spinal-Fluid

FMJClass II21 CFR 880.2500510(k) required6 decisions since 19884 recalls

6 FDA decisions since 1988. 4 recalls name this code, 0 of them Class I. The most-cited predicate is K032432, named by 1 later device.

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 hospital panel

Twenty years of FMJ 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 · FMJ

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMJ

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

Recalls per year · FMJ

No recall names FMJ since 2007.

Adverse event reports per year · FMJ

1in 2025

2007: 12009: 12010: 72011: 12012: 282013: 1012014: 1762015: 842019: 12023: 12025: 1
2007high 176 (2014) · low 0 (2008)2025

MAUDE reports naming product code FMJ, 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—00
20090—01
20100—07
20110—01
20120—028
20130—0101
20140—0176
20150—084
20160—00
20171—00
20180—00
20190—01
20200—00
20210—00
20220—00
20230—01
20240—00
20250—01
20260—0—
FIG. 1 — FMJ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FMJ? 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