SILVERSEAL— 510(k) K033587

Name: FDA 510(k) clearance K033587
Creator: U.S. Food and Drug Administration
Published: 2004-08-05

Substantially Equivalent

Noble Fiber Technologies

FDA 510(k) clearance K033587 for SILVERSEAL, Substantially Equivalent on 2004-08-05. Applicant: Noble Fiber Technologies. Device class: Unclassified.

Clearance details

Applicant: Noble Fiber Technologies
Product code: Code FRO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-11-13
Decision date: 2004-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarks Summit, PA, US

Download summary PDF View on FDA.gov ↗

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K033900 — X-STATIC SILVERSEAL HYDROCOLLOID FILM AND ISLAND DRESSING2005-01-14
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Adverse events under product code FRO

product code FRO

Death: 30
Injury: 653
Malfunction: 479
Other: 11
Total: 1,173

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.