FDA 510(k) Applications Submitted by STURDY INDUSTRIAL CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032596 | 08/22/2003 | STURDY MANUAL RESUSCITATOR | STURDY INDUSTRIAL CO., LTD |
| K231489 | 05/23/2023 | Sturdy Autoclave Super Microm | Sturdy Industrial Co., Ltd |
| K181993 | 07/26/2018 | STURDY Autoclave Super Microm (models SA-260MA and SA-260MA-R) | Sturdy Industrial Co., Ltd |
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