HERRICK LACRIMAL PLUG TM.— 510(k) K896175

Name: FDA 510(k) clearance K896175
Creator: U.S. Food and Drug Administration
Published: 1990-01-22

Substantially Equivalent

Lacrimedics, Inc.

FDA 510(k) clearance K896175 for HERRICK LACRIMAL PLUG TM., Substantially Equivalent on 1990-01-22. Applicant: Lacrimedics, Inc.. Device class: Unclassified.

Clearance details

Applicant: Lacrimedics, Inc.
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-10-25
Decision date: 1990-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rosemead, CA, US

Download summary PDF View on FDA.gov ↗

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K161673 — LacriPro Punctum Plug2016-11-18
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K030300 — OPAQUE HERRICK LACRIMAL PLUG2003-05-09
K021831 — OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPB2002-07-01
K001737 — OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM2000-06-19

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.