510(k) Report

FDA product code · Obstetrics and gynecology

Fluid, Hysteroscopy

LTAClass IIIPMA required2 decisions since 19750 recalls

2 FDA decisions since 1975. No recall names this code.

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, obstetrics and gynecology panel

Twenty years of LTA 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 · LTA

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LTA

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

Recalls per year · LTA

No recall names LTA since 2007.

Adverse event reports per year · LTA

3in 2014

2007: 12014: 3
2007high 3 (2014) · low 0 (2008)2025

MAUDE reports naming product code LTA, 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
20081—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—03
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — LTA by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LTA? 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