510(k) Report

FDA product code · Microbiology

Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples

SANClass II21 CFR 866.1650510(k) required8 decisions since 20240 recalls

8 FDA decisions since 2024. 510(k) reviews decided 2021–2025 took a median of 468 days (half between 166 and 686). No recall names this code. The most-cited predicate is K211815, named by 2 later devices.

Automated system that performs antimicrobial susceptibility testing using positive blood culture samples

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 SAN 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 · SAN

1in 2025

2024: 42025: 12026 (partial year): 3
2007high 4 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · SAN

577in 2024

2024: 577 days median2026 (partial year): 169 days median
2007high 577 (2024)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · SAN

No recall names SAN since 2007.

Adverse event reports per year · SAN

No MAUDE report names SAN 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
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
2024457700
20251—00
202631690—
FIG. 1 — SAN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in SAN? 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 866.1650.