SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG— 510(k) K020882

Name: FDA 510(k) clearance K020882
Creator: U.S. Food and Drug Administration
Published: 2002-07-26

Substantially Equivalent

Surgical Specialties Corp

FDA 510(k) clearance K020882 for SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG, Substantially Equivalent on 2002-07-26. Applicant: Surgical Specialties Corp. Device class: Unclassified.

Clearance details

Applicant: Surgical Specialties Corp
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-03-18
Decision date: 2002-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Reading, PA, 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.