K243138
- 510(k) number
- K243138
- Device name
- Geon (S2) Nasal Aspirator
- Applicant
- Geon Corporation TW
- Product code
- BTA — Pump, Portable, Aspiration (Manual Or Powered)
- Decision date
- 2025-02-04
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K243138.pdf
Official FDA record: K243138
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.