RTVUE— 510(k) K062552
Substantially EquivalentOptovue, Inc.
FDA 510(k) clearance K062552 for RTVUE, Substantially Equivalent on 2006-10-06. Applicant: Optovue, Inc.. Device class: 2.
Clearance details
- Applicant
- Optovue, Inc.
- Product code
- Code OBO
- Device class
- Class 2
- Regulation
- 21 CFR 886.1570
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fremont, CA, US
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