Sims Portex, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K011925 | HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE; HYPODERMIC NEEDLE-PRO SYRINGE & NEEDLE WITH NEEDLE PROTECTIO | FMI | 2001-07-12 | View |
| 510(k) | K002201 | ELECTROSTATIC HYDROPHOBIC BREATHING FILTER | CAH | 2001-02-05 | View |
| 510(k) | K002506 | BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT | CAH | 2000-12-14 | View |
| 510(k) | K001318 | CPAP SYSTEM, MODEL 102001 | BYE | 2000-07-20 | View |
| 510(k) | K993619 | CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCK | BSP | 2000-04-28 | View |
| 510(k) | K994275 | SIMS PORTEX ANESTHESIA CATHETER | FRN | 2000-02-22 | View |
| 510(k) | K991861 | 1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC MANUAL RESUSCITATOR, BAG RESERVOIR, 1ST RE | BTM | 2000-01-18 | View |
| 510(k) | K992471 | SIMS PORTEX EPIDURAL CATHETER, 20G MODEL# 4910-16/17; 21G MODEL# 4910-18 | BSO | 1999-10-22 | View |
| 510(k) | K992057 | IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006 | BTM | 1999-09-13 | View |
| 510(k) | K983858 | SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES | MIA | 1999-01-29 | View |
| 510(k) | K981035 | PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES | JKA | 1998-04-21 | View |
| 510(k) | K980466 | PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT WITH SPECIALTY TRACHEOSTOMY TUBE AND DISPOSABLE INNER CANNULA | JOH | 1998-02-24 | View |
No matching devices.
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