ANGIOPLUS-S— 510(k) K843972

Name: FDA 510(k) clearance K843972
Creator: U.S. Food and Drug Administration
Published: 1985-01-03

Substantially Equivalent

Oec-Diasonics, Inc.

FDA 510(k) clearance K843972 for ANGIOPLUS-S, Substantially Equivalent on 1985-01-03. Applicant: Oec-Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Oec-Diasonics, Inc.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1984-10-11
Decision date: 1985-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JAA

product code JAA

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.