Vitalograph (Ireland) , Ltd.
Vitalograph (Ireland) , Ltd. appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 26, 2016.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 2
- Compliance Actions
- 0
Known Names
Vitalograph (Ireland), Vitalograph Ireland
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K160253 | Vitalograph Model 6300 micro | Aug 26, 2016 |
| K142642 | Vitalograph Model 6600 Compact | Jun 30, 2015 |
| K142812 | Vitalograph Model 6800 Pneumotrac | Jun 29, 2015 |
| K141546 | VITALOGRAPH MODEL 7000 SPIROTRAC | Sep 3, 2014 |
| K110525 | VITALOGRAPH MODEL 7100 - VITALOJAK | Nov 23, 2011 |
| K100687 | VITALOGRAPH HAND HELD SPIROMETER, MODEL 2120 | Oct 16, 2010 |
| K073155 | VITALOGRAPH MODEL 4000 (ASMA-1 AND COPD-6) | Jun 4, 2008 |