Bausch + Lomb Boston Scleral Lens Case— 510(k) K173365
Substantially EquivalentBausch & Lomb, Incorporated
FDA 510(k) clearance K173365 for Bausch + Lomb Boston Scleral Lens Case, Substantially Equivalent on 2017-11-17. Applicant: Bausch & Lomb, Incorporated.
Clearance details
- Applicant
- Bausch & Lomb, Incorporated
- Product code
- Code LRX
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rochester, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.