LINEAR ARRAY TRANSDUCER OR SCANHEAD— 510(k) K840408

Name: FDA 510(k) clearance K840408
Creator: U.S. Food and Drug Administration
Published: 1984-04-25

Substantially Equivalent

Adr Ultrasound

FDA 510(k) clearance K840408 for LINEAR ARRAY TRANSDUCER OR SCANHEAD, Substantially Equivalent on 1984-04-25. Applicant: Adr Ultrasound. Device class: 2.

Clearance details

Applicant: Adr Ultrasound
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1984-01-31
Decision date: 1984-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.