Luther Medical Products, Inc.
FDA 510(k) & PMA Approved Devices — 17 products
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Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K982797 | BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB | DYB | 1998-11-30 | View |
| 510(k) | K980090 | ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM) | LJS | 1998-03-24 | View |
| 510(k) | K974543 | L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGER | FOZ | 1998-02-10 | View |
| 510(k) | K940198 | L-CATH CONNECTOR ASSEMBLY | GCD | 1994-12-15 | View |
| 510(k) | K942103 | L-CATH CATHETER SYSTEM - PORT L-CATH | LJT | 1994-07-26 | View |
| 510(k) | K930473 | ONECATH L-CATH CATHETER SYSTEM | LJS | 1994-04-07 | View |
| 510(k) | K925236 | L CATH(R) CATHETER SYSTEM | LJS | 1994-03-22 | View |
| 510(k) | K920755 | L-CATH PEEL AWAY SYSTEM CATHETER | LJS | 1993-06-07 | View |
| 510(k) | K925979 | DUAL LUMEN L-CATH CATHETER SYSTEM | DQX | 1993-05-27 | View |
| 510(k) | K924968 | L-CATH PEEL-AWAY CATHETER SYSTEM | FOZ | 1993-05-21 | View |
| 510(k) | K924562 | CATHETER INTRODUCER | DYB | 1993-02-25 | View |
| 510(k) | K884806 | LUMED EXPANDO-CATH, ACTIV | FOZ | 1989-02-08 | View |
| 510(k) | K871546 | SAFESIDE(TM) LUMED | FOZ | 1987-06-17 | View |
| 510(k) | K853348 | L-CATH EXPANDO CATH | FOZ | 1986-01-09 | View |
| 510(k) | K822217 | THERMOTHERAPY | LKX | 1982-09-24 | View |
| 510(k) | K820102 | SUBCLAVIAN JUGULAR CATHETER SET | DQR | 1982-01-29 | View |
| 510(k) | K801575 | L-CATH INTRAVENOUS PLACEMENT UNIT | FOZ | 1980-08-20 | View |
No matching devices.
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