Michigan Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 7
- Inspections
- 5
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1632-2018 | Class III | Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device i | February 13, 2018 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K073079 | THUMPER, MODEL: 1008 | February 14, 2008 |
| K972525 | THUMPER | October 2, 1997 |
| K962237 | THUMPER CARDIOPULMONARY RESUSCITATOR | September 5, 1996 |
| K895954 | LARYNGOSTAT LARYNGOSCOPE HANDLE | October 30, 1989 |
| K851139 | THUMPER CARDIOPULMONARY RESUSCITATOR 1005 | May 15, 1985 |
| K833879 | CARDIOPULMONARY RESUSCITATOR | December 27, 1983 |
| K811909 | CARDIOPULMUNARY RESUSCITATOR | July 16, 1981 |