Verily Numetric Retinal Camera— 510(k) K242508
Substantially EquivalentVerily Life Sciences, LLC
FDA 510(k) clearance K242508 for Verily Numetric Retinal Camera, Substantially Equivalent on 2024-12-09. Applicant: Verily Life Sciences, LLC. Device class: 2.
Clearance details
- Applicant
- Verily Life Sciences, LLC
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- South San Francisco, CA, US
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