Vas-Cath of Canada , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 19
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K875188 | LUER LOCK CONNECTORS / RIDIG P.V.C. | March 2, 1988 |
| K871817 | VAS-CATH PERITONEAL DIALYSIS CATHETER | July 16, 1987 |
| K871488 | VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH | June 12, 1987 |
| K871487 | VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH | June 12, 1987 |
| K863982 | VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY | October 24, 1986 |
| K853283 | VACCESS TM 4006 | August 22, 1985 |
| K844854 | OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT | May 21, 1985 |
| K844800 | OPTI-FLOW & OPTI-TORQUE ANGIOGRAPHIC CATHETERS | May 16, 1985 |
| K850009 | EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER | May 13, 1985 |
| K844434 | VACCESS 3000 SINGLE LUMEN JUGULAR CANNULA-CATH | March 13, 1985 |
| K844336 | VAS-CATH PARALLEL DUAL LUMAN JUGULAR CANNUAL CATH | March 13, 1985 |
| K844433 | VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA | March 13, 1985 |
| K844982 | VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY | January 18, 1985 |
| K842864 | VACCESS FEMORAL CANNULA | August 8, 1984 |
| K834232 | VAS-CATH DSA CATHETER/TRAY | April 24, 1984 |
| K840322 | HEMOFILTRATION CATHETER HF-100 | April 24, 1984 |
| K834358 | PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA | April 2, 1984 |
| K810745 | DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 | March 31, 1981 |
| K791308 | ULDALL SUBCLAVIAN CANNULA SC-100 | August 3, 1979 |