Manner Medical Products
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K760219 | MASKA, OXYGEN VINYL D-SP. SINGLE USE | August 3, 1976 |
| K760220 | TUBING, SINGLE USE OXYGEN SUPPLY | August 3, 1976 |
| K760221 | I.P.P.B., DIS. W/MANIFOLD/NEBULIZER | August 3, 1976 |
| K760218 | CANNULAE, PLASTIC DISPOSABLE NASAL | August 3, 1976 |