Atlas FDA

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

Liaoning-Usa Corp. · Predicate Candidate Screening

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

134 daysmedian FDA review time
163 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K911921DISPOSABLE ISOLATION GOWNLiaoning-Usa Corp.1991-05-13130
K905487VARIOUS TYPES OF STETHOSCOPESLiaoning-Usa Corp.1991-04-091240
K910623GAUZE SPONGES ABSORBENT GAUZE ROLLSLiaoning-Usa Corp.1991-04-01470
K902625CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPITLiaoning-Usa Corp.1990-10-261340
K892781ANTELOPE BRAND PATIENT EXAMINATION GLOVESLiaoning-Usa Corp.1989-09-211630
K892774PATIENT EXAMINATION GLOVESLiaoning-Usa Corp.1989-09-131550

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