Class Class II

Altaviz Intravitreal Syringe (K243322)

K243322 2025-05-09 Traditional
Home/ Devices/ Altaviz Intravitreal Syringe (K243322)

Description

Altaviz Intravitreal Syringe by Altaviz, LLC, an FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243322
Clearance Date2025-05-09
Clearance TypeTraditional
Product CodeQLY
Regulation Number880.5860

Categories

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