Life Design Systems, Inc.
FDA 510(k) & PMA Approved Devices — 29 products
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Total Devices29
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K913714 | MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM) | BTM | 1992-12-01 | View |
| 510(k) | K885313 | HUMIDI-FLEX TM | BYD | 1989-10-11 | View |
| 510(k) | K893030 | CHILD SIZE - FILTER FLEX (TM) | CAH | 1989-09-18 | View |
| 510(k) | K892862 | FLEX-CUP PERCUSSOR | BYI | 1989-05-25 | View |
| 510(k) | K892221 | PULMONARY RESUSCITATOR, MODIFICATION | BTM | 1989-05-18 | View |
| 510(k) | K890011 | OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING | BZO | 1989-03-20 | View |
| 510(k) | K890108 | MODIFIED CUSHION-FLEX(TM) | BSJ | 1989-01-24 | View |
| 510(k) | K884387 | CUSHION FLEX(TM) | BSJ | 1988-11-17 | View |
| 510(k) | K884068 | PULMANEX TM (NEO-NATAL SIZE) | BTM | 1988-11-16 | View |
| 510(k) | K873179 | HEATER WIRE BREATHING CIRCUIT | BZE | 1988-03-31 | View |
| 510(k) | K863857 | PULSE-OX | DQA | 1987-10-07 | View |
| 510(k) | K864681 | CARHILL ONE-WAY RESUSCITATION VALVE | CBP | 1987-05-21 | View |
| 510(k) | K871669 | BABYSET(TM) MODIFIED JACKSON-REES CIRCUIT W/VALVE | CAI | 1987-05-19 | View |
| 510(k) | K862448 | FLOW GENERATOR FOR SLEEP APNEA, LDS 1500 | BZD | 1986-11-14 | View |
| 510(k) | K863026 | PULMANEX TM (MODIFICATION) | BTM | 1986-08-26 | View |
| 510(k) | K861758 | CUSHION-FLEX TM NASAL CPAP MASK FOR SLEEP APNEA | BYE | 1986-07-14 | View |
| 510(k) | K860659 | END TIDAL CO2 SAMPLING CIRCUIT | BZO | 1986-04-17 | View |
| 510(k) | K860693 | PULMANEX (TM) | BTM | 1986-03-27 | View |
| 510(k) | K854822 | LDS PEEP VALVE | BYE | 1986-02-24 | View |
| 510(k) | K854458 | CUSHION-FLEX TM-CPAP FACE MASK | BYE | 1986-01-15 | View |
No matching devices.
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