Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Wright Linear Pump, Inc. — Predicate Candidate Screening

6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

181 daysmedian FDA review time
216 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K071040WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMSWright Linear Pump, Inc.2007-05-22400
K961797WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITEWright Linear Pump, Inc.1996-11-061810
K961891WLP SINGLE-SEGMENT VERSION WLP SOLO VIIWright Linear Pump, Inc.1996-11-061810
K961292WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAWright Linear Pump, Inc.1996-11-062160
K883186WRIGHT GRADIENT PRESSURE SUPPORT STOCKINGSWright Linear Pump, Inc.1988-11-211160
K830577LINEAR PUMP #4370975Wright Linear Pump, Inc.1983-05-25910

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