510(k) Report

FDA product code · Neurology

Impedance Plethysmograph, Cranial

QAFClass II21 CFR 870.2770510(k) required3 decisions since 20170 recalls

3 FDA decisions since 2017. No recall names this code. The most-cited predicate is K182967, named by 1 later device.

Detect or measure variations in volume in the cranium, using tissue impedance properties.

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, neurology panel

Twenty years of QAF 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 · QAF

1in 2018

2017: 12018: 12026 (partial year): 1
2007high 1 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QAF

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

Recalls per year · QAF

No recall names QAF since 2007.

Adverse event reports per year · QAF

No MAUDE report names QAF since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20171—00
20181—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20261—0—
FIG. 1 — QAF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QAF? 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 870.2770.