FDA 510(k) Applications Submitted by Bosungmeditech Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230759 | 03/20/2023 | SafeLan« (2 models/SafeLan 26G, SafeLan 30G), SafeLan«-Pro (1 model/SafeLan«-Pro) | Bosungmeditech Co., Ltd. |
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