OcuMet Beacon (OCUB100)— 510(k) K241931
Substantially EquivalentOcusciences, Inc.
FDA 510(k) clearance K241931 for OcuMet Beacon (OCUB100), Substantially Equivalent on 2025-04-22. Applicant: Ocusciences, Inc.. Device class: 2.
Clearance details
- Applicant
- Ocusciences, Inc.
- Product code
- Code MYC
- Device class
- Class 2
- Regulation
- 21 CFR 886.1570
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ann Arbor, MI, US
Recent devices under product code MYC
view allData sourced from openFDA. This site is unofficial and independent of the FDA.