DELTA PUNCTUM PLUG— 510(k) K050851

Name: FDA 510(k) clearance K050851
Creator: U.S. Food and Drug Administration
Published: 2005-08-19

Substantially Equivalent

Delta Life Science, Inc.

FDA 510(k) clearance K050851 for DELTA PUNCTUM PLUG, Substantially Equivalent on 2005-08-19. Applicant: Delta Life Science, Inc.. Device class: Unclassified.

Clearance details

Applicant: Delta Life Science, Inc.
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 2005-04-04
Decision date: 2005-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

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K162361 — Soft Plug Extended Duration 180 Canalicular Plug2017-04-17

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.