ULTRASOUND SCANNER PROFOCUS, MODEL 2202— 510(k) K070077

Name: FDA 510(k) clearance K070077
Creator: U.S. Food and Drug Administration
Published: 2007-03-05

Substantially Equivalent

B-K Medical Aps

FDA 510(k) clearance K070077 for ULTRASOUND SCANNER PROFOCUS, MODEL 2202, Substantially Equivalent on 2007-03-05. Applicant: B-K Medical Aps. Device class: 2.

Clearance details

Applicant: B-K Medical Aps
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 2007-01-08
Decision date: 2007-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herlev, DK

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.