TEAR VOLUME TESTS— 510(k) K881515
Substantially EquivalentVisionex, Inc.
FDA 510(k) clearance K881515 for TEAR VOLUME TESTS, Substantially Equivalent on 1988-05-23. Applicant: Visionex, Inc.. Device class: 1.
Clearance details
- Applicant
- Visionex, Inc.
- Product code
- Code KYD
- Device class
- Class 1
- Regulation
- 21 CFR 886.1800
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sunnyvale, CA, US
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