Glaxosmithkline Consumer Healthcare
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K093189 | ACTIPROTECT UC N95 RESPIRATOR | July 2, 2010 |
| K093161 | ACTIPROTECT UF N95 RESPIRATOR | May 10, 2010 |
| K081923 | ACTIPROTECT UF N95 RESPIRATOR, DOUBLE STRAP, FLAT FOLD | July 1, 2009 |