RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION— 510(k) K020802
Substantially EquivalentBausch & Lomb, Incorporated
FDA 510(k) clearance K020802 for RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION, Substantially Equivalent on 2002-05-31. Applicant: Bausch & Lomb, Incorporated. Device class: 2.
Clearance details
- Applicant
- Bausch & Lomb, Incorporated
- Product code
- Code LYL
- Device class
- Class 2
- Regulation
- 21 CFR 886.5928
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rochester, NY, US
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Adverse events under product code LYL
product code LYL- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.