Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vas-Cath of Canada , Ltd. — Predicate Candidate Screening
19 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
76 daysmedian FDA review time
156 days90th percentile
19clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K875188 | LUER LOCK CONNECTORS / RIDIG P.V.C. | Vas-Cath of Canada , Ltd. | 1988-03-02 | 76 | 0 |
| K871817 | VAS-CATH PERITONEAL DIALYSIS CATHETER | Vas-Cath of Canada , Ltd. | 1987-07-16 | 66 | 0 |
| K871488 | VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH | Vas-Cath of Canada , Ltd. | 1987-06-12 | 58 | 0 |
| K871487 | VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH | Vas-Cath of Canada , Ltd. | 1987-06-12 | 58 | 0 |
| K863982 | VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY | Vas-Cath of Canada , Ltd. | 1986-10-24 | 10 | 0 |
| K853283 | VACCESS TM 4006 | Vas-Cath of Canada , Ltd. | 1985-08-22 | 17 | 0 |
| K844854 | OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT | Vas-Cath of Canada , Ltd. | 1985-05-21 | 159 | 0 |
| K844800 | OPTI-FLOW & OPTI-TORQUE ANGIOGRAPHIC CATHETERS | Vas-Cath of Canada , Ltd. | 1985-05-16 | 156 | 0 |
| K850009 | EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER | Vas-Cath of Canada , Ltd. | 1985-05-13 | 131 | 0 |
| K844336 | VAS-CATH PARALLEL DUAL LUMAN JUGULAR CANNUAL CATH | Vas-Cath of Canada , Ltd. | 1985-03-13 | 125 | 0 |
| K844434 | VACCESS 3000 SINGLE LUMEN JUGULAR CANNULA-CATH | Vas-Cath of Canada , Ltd. | 1985-03-13 | 117 | 0 |
| K844433 | VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA | Vas-Cath of Canada , Ltd. | 1985-03-13 | 117 | 1 |
| K844982 | VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY | Vas-Cath of Canada , Ltd. | 1985-01-18 | 23 | 0 |
| K842864 | VACCESS FEMORAL CANNULA | Vas-Cath of Canada , Ltd. | 1984-08-08 | 16 | 0 |
| K840322 | HEMOFILTRATION CATHETER HF-100 | Vas-Cath of Canada , Ltd. | 1984-04-24 | 90 | 0 |
| K834232 | VAS-CATH DSA CATHETER/TRAY | Vas-Cath of Canada , Ltd. | 1984-04-24 | 140 | 0 |
| K834358 | PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA | Vas-Cath of Canada , Ltd. | 1984-04-02 | 111 | 0 |
| K810745 | DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 | Vas-Cath of Canada , Ltd. | 1981-03-31 | 12 | 0 |
| K791308 | ULDALL SUBCLAVIAN CANNULA SC-100 | Vas-Cath of Canada , Ltd. | 1979-08-03 | 18 | 0 |
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