SOPRO 281— 510(k) K103813

Name: FDA 510(k) clearance K103813
Creator: U.S. Food and Drug Administration
Published: 2011-03-22

Substantially Equivalent

Sopro

FDA 510(k) clearance K103813 for SOPRO 281, Substantially Equivalent on 2011-03-22. Applicant: Sopro. Device class: 2.

Clearance details

Applicant: Sopro
Product code: Code NTN
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2010-12-29
Decision date: 2011-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Laurel, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NTN

product code NTN

Other: 1
Total: 1

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.