Altaviz Intravitreal Syringe— 510(k) K243322
Substantially EquivalentAltaviz, LLC
FDA 510(k) clearance K243322 for Altaviz Intravitreal Syringe, Substantially Equivalent on 2025-05-09. Applicant: Altaviz, LLC. Device class: 2.
Clearance details
- Applicant
- Altaviz, LLC
- Product code
- Code QLY
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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More clearances from Altaviz, LLC
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