Neoforce Group, Inc.
Neoforce Group, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 10, 2011.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K110119 | PRESSURE MANOMETER | June 10, 2011 |
| K103833 | NEOPIP PATIENT CIRCUIT WITH PEEP | April 20, 2011 |
| K102649 | NEOPOP INFANT RESUSCITATOR WITH FLOW METER | January 6, 2011 |
| K092085 | ISPIRA RESUSCITATION UNIT | October 7, 2009 |
| K072021 | NEOPIP INFANT RESUSCITATOR | September 12, 2007 |
| K070416 | NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP | May 29, 2007 |
| K061280 | V-2200 INFANT INCUBATOR | June 27, 2006 |