Sturdy Industrial Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K231489 | Sturdy Autoclave Super Microm | June 21, 2023 |
| K181993 | STURDY Autoclave Super Microm (models SA-260MA and SA-260MA-R) | November 1, 2019 |
| K032596 | STURDY MANUAL RESUSCITATOR | August 5, 2004 |