510(k) Report

FDA product code · Microbiology

Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igg

MYLClass IIIPMA required3 decisions since 19992 recalls

3 FDA decisions since 1999. 2 recalls name this code, 0 of them Class I.

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, microbiology panel

Twenty years of MYL 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 · MYL

7in 2025

2007: 32009: 12010: 12012: 12013: 12016: 12017: 32019: 12020: 22021: 12024: 42025: 72026 (partial year): 2
2007high 7 (2025) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MYL

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

Recalls per year · MYL

2in 2023

2023: 2
2007high 2 (2023) · low 0 (2007)2026

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

Adverse event reports per year · MYL

No MAUDE report names MYL since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20073—00
20080—00
20091—00
20101—00
20110—00
20121—00
20131—00
20140—00
20150—00
20161—00
20173—00
20180—00
20191—00
20202—00
20211—00
20220—00
20230—20
20244—00
20257—00
20262—0—
FIG. 1 — MYL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MYL? 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