GEL MARK V— 510(k) K050090

Name: FDA 510(k) clearance K050090
Creator: U.S. Food and Drug Administration
Published: 2005-02-07

Substantially Equivalent

Senorx, Inc.

FDA 510(k) clearance K050090 for GEL MARK V, Substantially Equivalent on 2005-02-07. Applicant: Senorx, Inc.. Device class: 2.

Clearance details

Applicant: Senorx, Inc.
Product code: Code NEU
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2005-01-14
Decision date: 2005-02-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Aliso Viejo, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NEU

product code NEU

Injury: 824
Total: 824

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.