TEAR VOLUME TESTS— 510(k) K881515

Substantially Equivalent

Visionex, 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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