DeviceClearance

WINDSURFER— 510(k) K050561

Substantially Equivalent

Medcon , Ltd.

FDA 510(k) clearance K050561 for WINDSURFER, Substantially Equivalent on 2005-05-04. Applicant: Medcon , Ltd.. Device class: 2.

Clearance details

Applicant
Medcon , Ltd.
Product code
Code DQK
Device class
Class 2
Regulation
21 CFR 870.1425
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Efrat, IL
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQK

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More clearances from Medcon , Ltd.

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Adverse events under product code DQK

product code DQK
Death
10
Injury
225
Malfunction
2,123
Other
2
Total
2,360

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 →

Recalls naming K050561

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K050561.

Data sourced from openFDA. This site is unofficial and independent of the FDA.