510(k) Report

FDA product code · Immunology

Antigen (Complexed),Prostate Specific,(Cpsa)

NAFClass IIIPMA required1 decision since 20000 recalls

1 FDA decision since 2000. 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, immunology panel

Twenty years of NAF 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 · NAF

1in 2025

2009: 32010: 12012: 12016: 12018: 22019: 12020: 42021: 12023: 12024: 22025: 1
2007high 4 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NAF

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

Recalls per year · NAF

No recall names NAF since 2007.

Adverse event reports per year · NAF

24in 2019

2007: 22008: 12010: 22011: 32013: 12019: 24
2007high 24 (2019) · low 0 (2009)2025

MAUDE reports naming product code NAF, 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—02
20080—01
20093—00
20101—02
20110—03
20121—00
20130—01
20140—00
20150—00
20161—00
20170—00
20182—00
20191—024
20204—00
20211—00
20220—00
20231—00
20242—00
20251—00
20260—0—
FIG. 1 — NAF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NAF? 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