OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM— 510(k) K001737

Substantially Equivalent

Lacrimedics, Inc.

FDA 510(k) clearance K001737 for OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM, Substantially Equivalent on 2000-06-19. Applicant: Lacrimedics, Inc..

Clearance details

Applicant: Lacrimedics, Inc.
Product code: Code LZU
Advisory panel: Unknown
Date received: 2000-06-07
Decision date: 2000-06-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Eastsound, WA, US

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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.