Smiths Industries Medical Systems, Inc.
FDA 510(k) & PMA Approved Devices — 22 products
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Total Devices22
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972385 | FENESTRATED FLEXIBLE D.I.C. TRACHEOSTOMY TUBE CUFFED | JOH | 1998-01-20 | View |
| 510(k) | K965017 | REGIONAL ANESTHESIA TRAYS | CAZ | 1997-03-14 | View |
| 510(k) | K962175 | PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE | JOH | 1997-01-17 | View |
| 510(k) | K962931 | SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT | JKA | 1996-10-21 | View |
| 510(k) | K963570 | SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) | FMJ | 1996-10-18 | View |
| 510(k) | K960429 | PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULA | JOH | 1996-05-02 | View |
| 510(k) | K953485 | SIMS CPAP SYSTEM | BYE | 1995-10-26 | View |
| 510(k) | K953483 | SIMS BLUE LINE ENDOBRONCHIAL TUBE | CBI | 1995-10-24 | View |
| 510(k) | K932947 | WALLACE Y-CAN | FOZ | 1995-09-01 | View |
| 510(k) | K932946 | WALLACE IV CANNULA | FOZ | 1995-09-01 | View |
| 510(k) | K952516 | PRO-VENT, LINE DRAW, PULSATOR | JKA | 1995-07-14 | View |
| 510(k) | K945777 | PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES | JKA | 1994-12-22 | View |
| 510(k) | K935927 | CONCORD/PORTEX EPIDURAL CATHETERS | BSO | 1994-09-09 | View |
| 510(k) | K942937 | SHARPSAFE CAT NO. 4105, 4115 AND 4120 | FMI | 1994-08-25 | View |
| 510(k) | K936133 | PERCUTANEOUS TRACHEOSTOMY KIT | JOH | 1994-03-23 | View |
| 510(k) | K935776 | SHARPSAFE, CAT. NO. 4126 | FMI | 1994-02-28 | View |
| 510(k) | K935777 | SHARPSAFE, CAT. NO. 4125 | FMI | 1994-02-28 | View |
| 510(k) | K935603 | EXTRACORPOREAL TEMPERATURE SENSOR | FLL | 1994-02-15 | View |
| 510(k) | K935628 | SHARPSAFE CAT. NO. 4127 | FMI | 1994-02-04 | View |
| 510(k) | K936134 | BERMAN AIRWAY | CAE | 1994-01-28 | View |
No matching devices.
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