TEAR VOLUME TESTS
K-Number: K881515 · 1988-05-23
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Device Summary
Frequently Asked Questions
What is the TEAR VOLUME TESTS?
TEAR VOLUME TESTS is a medical device that received FDA 510(k) clearance on 1988-05-23. The listed applicant is Visionex, Inc.. The 510(k) number is K881515.
When did TEAR VOLUME TESTS receive FDA 510(k) clearance?
TEAR VOLUME TESTS received FDA 510(k) clearance on 1988-05-23, under 510(k) number K881515.
Who is the listed applicant for TEAR VOLUME TESTS?
The FDA 510(k) record lists Visionex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEAR VOLUME TESTS?
The FDA product code for TEAR VOLUME TESTS is KYD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Visionex, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KYD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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