Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

PIW — Predicate Candidate Screening

9 FDA 510(k) clearances under this product code; the 50 most recent screened below.

144 daysmedian FDA review time
181 days90th percentile
9clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K243426Nurochek-Pro SystemHeadsafe Mfg Pty, Ltd.2025-03-271430
K231914Nurochek-II SystemHeadsafe Mfg Pty, Ltd.2023-12-271810
K190815BrainScope TBIBrainscope Company, Inc.2019-09-111660
K183241BrainScope TBI (Model: Ahead 400)Brainscope Company, Inc.2019-02-19900
K181785Modified BrainScope OneBrainscope Company, Inc.2018-12-191690
K181179BrainScope OneBrainscope Company, Inc.2018-05-18160
K161068Ahead 300Brainscope Company, Inc.2016-09-221600
K143643Brainscope Ahead 200Brainscope Company, Inc.2015-05-151440
DEN140025BrainScope Ahead 100Brainscope Company, Inc.2014-11-17890

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda