LACRIMAL EFFICIENCY TEST (TM)— 510(k) K890714

Name: FDA 510(k) clearance K890714
Creator: U.S. Food and Drug Administration
Published: 1989-05-17

Substantially Equivalent

Lacrimedics, Inc.

FDA 510(k) clearance K890714 for LACRIMAL EFFICIENCY TEST (TM), Substantially Equivalent on 1989-05-17. Applicant: Lacrimedics, Inc.. Device class: Unclassified.

Clearance details

Applicant: Lacrimedics, Inc.
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-02-13
Decision date: 1989-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rosemead, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LZU

product code LZU

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.