510(k) Report

FDA product code · Immunology

Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

MTGClass IIIPMA required7 decisions since 19952 recalls

7 FDA decisions since 1995. 2 recalls name this code, 0 of them Class I. The most-cited predicate is P950021, 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, immunology panel

Twenty years of MTG 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 · MTG

6in 2025

2007: 72008: 72009: 32010: 92011: 252012: 172013: 122014: 132015: 72016: 32017: 92018: 72019: 92020: 132021: 72022: 42023: 92024: 32025: 62026 (partial year): 6
2007high 25 (2011) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MTG

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

Recalls per year · MTG

1in 2011

2008: 12011: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · MTG

20in 2025

2011: 32012: 42013: 32014: 12015: 92016: 52017: 82018: 122019: 132020: 62021: 92022: 42023: 52024: 82025: 20
2007high 20 (2025) · low 0 (2007)2025

MAUDE reports naming product code MTG, 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
20077—00
20087—10
20093—00
20109—00
201125—13
201217—04
201312—03
201413—01
20157—09
20163—05
20179—08
20187—012
20199—013
202013—06
20217—09
20224—04
20239—05
20243—08
20256—020
20266—0—
FIG. 1 — MTG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MTG? 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