K243322
- 510(k) number
- K243322
- Device name
- Altaviz Intravitreal Syringe
- Applicant
- Altaviz, LLC CA · US
- Product code
- QLY — Ophthalmic Syringe
- Decision date
- 2025-05-09
- Date received
- 2024-10-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K243322.pdf
Official FDA record: K243322
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.