K232831
- 510(k) number
- K232831
- Device name
- Quiver Aspiration Pump
- Applicant
- Anoxia Medical, Inc. CA · US
- Product code
- BTA — Pump, Portable, Aspiration (Manual Or Powered)
- Decision date
- 2024-02-22
- Date received
- 2023-09-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K232831.pdf
Official FDA record: K232831
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.