Retitrack— 510(k) K222484
Substantially EquivalentC. Light Technologies, Inc.
FDA 510(k) clearance K222484 for Retitrack, Substantially Equivalent on 2023-05-09. Applicant: C. Light Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- C. Light Technologies, Inc.
- Product code
- Code HLL
- Device class
- Class 2
- Regulation
- 21 CFR 886.1510
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Medford, MA, US
Recent devices under product code HLL
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