CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENS— 510(k) K080632
Substantially EquivalentClearlab SG Pte, Ltd.
FDA 510(k) clearance K080632 for CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENS, Substantially Equivalent on 2008-10-15. Applicant: Clearlab SG Pte, Ltd.. Device class: 2.
Clearance details
- Applicant
- Clearlab SG Pte, Ltd.
- Product code
- Code MVN
- Device class
- Class 2
- Regulation
- 21 CFR 886.5925
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Junction, CO, US
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More clearances from Clearlab SG Pte, Ltd.
view allAdverse events under product code MVN
product code MVN- Injury
- 149
- Total
- 149
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.