Chemetron Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K781706 | RESPIRATOR/GILL 1/SIMV | January 22, 1979 |
| K781542 | HEATED NEBULIZER | October 10, 1978 |
| K781537 | NEBULIZER/HUMIDIFIER | October 10, 1978 |
| K781541 | FLOMETER | September 26, 1978 |