Neoforce Group, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K110119 | PRESSURE MANOMETER | CAP | 2011-06-10 | View |
| 510(k) | K103833 | NEOPIP PATIENT CIRCUIT WITH PEEP | BYE | 2011-04-20 | View |
| 510(k) | K102649 | NEOPOP INFANT RESUSCITATOR WITH FLOW METER | BTM | 2011-01-06 | View |
| 510(k) | K092085 | ISPIRA RESUSCITATION UNIT | BTL | 2009-10-07 | View |
| 510(k) | K072021 | NEOPIP INFANT RESUSCITATOR | BTM | 2007-09-12 | View |
| 510(k) | K070416 | NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP | BYE | 2007-05-29 | View |
| 510(k) | K061280 | V-2200 INFANT INCUBATOR | FMZ | 2006-06-27 | View |
No matching devices.
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