Atlas FDA

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

Jufrey Multimed Corp. — Predicate Candidate Screening

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

34 daysmedian FDA review time
46 days90th percentile
7clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K861518UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)Jufrey Multimed Corp.1986-05-27340
K861520UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205)Jufrey Multimed Corp.1986-05-27340
K861523STANDARD BLOOD TRANSFUSION FILTER SET (CODE 1025)Jufrey Multimed Corp.1986-05-27340
K861521UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330)Jufrey Multimed Corp.1986-05-27340
K861519UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)Jufrey Multimed Corp.1986-05-27340
K853527JUFREY CORP. UNIV. DISPOS. SCALP VEIN INFUSION SETJufrey Multimed Corp.1985-09-23460
K853327JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSIONJufrey Multimed Corp.1985-08-21130

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