K232702
- 510(k) number
- K232702
- Device name
- Solo+ Tympanostomy Tube Device (TTD)
- Applicant
- Aventamed Dac IE
- Product code
- ETD — Tube, Tympanostomy
- Decision date
- 2024-05-20
- Date received
- 2023-09-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232702.pdf
Official FDA record: K232702
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.