FDA 510(k) Applications Submitted by Spiggle & Theis Medizintechnik GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223542 | 11/25/2022 | TubaVent Balloon Dilatation System | Spiggle & Theis Medizintechnik GmbH |
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