FUKUDA DENSHI MODEL UF-850XTD— 510(k) K050363

Substantially Equivalent

Fukuda Denshi USA, Inc.

FDA 510(k) clearance K050363 for FUKUDA DENSHI MODEL UF-850XTD, Substantially Equivalent on 2005-02-17. Applicant: Fukuda Denshi USA, Inc..

Clearance details

Applicant
Fukuda Denshi USA, Inc.
Product code
Code IYN
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Redmond, WA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code IYN

product code IYN
Death
25
Injury
163
Malfunction
1,538
Other
4
Total
1,730

Source: openFDA MAUDE database, through . 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.