Daig Corp.
FDA 510(k) & PMA Approved Devices — 63 products
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Total Devices63
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K000004 | ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509 | DYB | 2000-11-29 | View |
| 510(k) | K994334 | ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXX | DYB | 2000-05-15 | View |
| 510(k) | K982299 | SPYGLASS 5 FR ANGIOGRAPHIC CATHETER | DQO | 1998-10-19 | View |
| 510(k) | K982187 | FAST-CATH INTRA-CARDIAC INTRODUCER | DYB | 1998-09-16 | View |
| 510(k) | K973840 | FAST-CATH (TM) INTRA-CARDIAC INTRODUCER | DYB | 1998-05-21 | View |
| 510(k) | K964518 | FAST-CATH TRANSSEPTAL CATHETER INTRODUCER | DYB | 1997-05-14 | View |
| 510(k) | K965249 | SPYGLASS ANGIOGRAPHIC CATHETER | DQO | 1997-02-21 | View |
| 510(k) | K962805 | SPYGLASS ANGIOGRAPHIC CATHETER | DQO | 1996-10-15 | View |
| 510(k) | K954317 | DIAG FAST-CATH DUO & TRIO REMOVABLE HEMOSTASIS ADAPTERS W/SIDEPORTS & 3-WAY STOPCOCKS | DYB | 1995-11-28 | View |
| 510(k) | K944284 | CONTROL | DQO | 1995-03-03 | View |
| 510(k) | K942379 | DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER | DRF | 1994-12-27 | View |
| 510(k) | K934285 | CATHETER INTRODUCER MODIFICATION | DYB | 1993-11-24 | View |
| 510(k) | K913940 | RESPONSE(TM) STEERABLE CATHETER | DRA | 1993-01-26 | View |
| 510(k) | K920779 | FAST-CATH HEMOSTASIS INTRODUCER | DYB | 1992-06-03 | View |
| 510(k) | K920327 | DAIG FAST CATH TRANSSEPTAL SHEATH INTRODUCER | DYB | 1992-04-16 | View |
| 510(k) | K914278 | DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN | DRF | 1992-03-04 | View |
| 510(k) | K914185 | PACEL(TM) FLOW DIRECTED PACING CATHETER | LDF | 1992-01-27 | View |
| 510(k) | K914090 | DAIG FAST CATH(TM) INTRODUCER, MODIFICATION | DYB | 1991-10-28 | View |
| 510(k) | K910861 | PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK | DYB | 1991-05-07 | View |
| 510(k) | K892528 | FIVE-YEAR STERILE PACKAGING SHELF LIFE | DTB | 1990-01-18 | View |
No matching devices.
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