Concord/Portex
FDA 510(k) & PMA Approved Devices — 23 products
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Total Devices23
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K923559 | STERI-CATH MDI | CAF | 1993-10-25 | View |
| 510(k) | K930218 | SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES | MAJ | 1993-07-27 | View |
| 510(k) | K924541 | EPIDURAL MINIPACK | BYO | 1993-07-09 | View |
| 510(k) | K930286 | DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS | CBT | 1993-06-22 | View |
| 510(k) | K923127 | NEEDLE-PRO CARTRIDGE | FMI | 1993-04-29 | View |
| 510(k) | K923910 | HEAT MOISTURE CONDENSER | BYD | 1993-01-26 | View |
| 510(k) | K922749 | LOW PROFILE TRACHEOSTOMY TUBE | BTO | 1992-09-02 | View |
| 510(k) | K922445 | VACU-PRO | JKA | 1992-08-12 | View |
| 510(k) | K915452 | ANESTHESIA BREATHING CIRCUIT | CAI | 1992-02-14 | View |
| 510(k) | K911809 | NEW-VENT | JKA | 1991-08-26 | View |
| 510(k) | K912124 | TRACHEOSTOMY TUBE AND CUFF | BTO | 1991-08-16 | View |
| 510(k) | K912043 | ACCU-VENT(TM) WITH NEEDLE-PRO(TM) | CBT | 1991-07-05 | View |
| 510(k) | K911638 | SYRINGE TIP CAP | JKA | 1991-06-21 | View |
| 510(k) | K911037 | SAFETY NEEDLE SHEATH, MODIFICATION | FMI | 1991-05-03 | View |
| 510(k) | K905011 | ORAL PHARYNGEAL CLEANSING DEVICE | EIA | 1991-01-31 | View |
| 510(k) | K904198 | SAFETY NEEDLE SHEATH | FMI | 1990-12-19 | View |
| 510(k) | K903730 | D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES | BTO | 1990-09-25 | View |
| 510(k) | K902687 | STERI-CATH-DL | BSY | 1990-08-29 | View |
| 510(k) | K902116 | MODIFIED ENDOBRONCHIAL TUBE | BTS | 1990-08-03 | View |
| 510(k) | K902383 | STERI-CATH(TM) | BSY | 1990-07-12 | View |
No matching devices.
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