ALL SILICONE FOLEY CATHETER, 2-WAY, 3-WAY, WITH TEMPERATURE SENSOR— 510(k) K063442

Substantially Equivalent

Degania Silicone , Ltd.

FDA 510(k) clearance K063442 for ALL SILICONE FOLEY CATHETER, 2-WAY, 3-WAY, WITH TEMPERATURE SENSOR, Substantially Equivalent on 2007-03-26. Applicant: Degania Silicone , Ltd.. Device class: 2.

Clearance details

Applicant
Degania Silicone , Ltd.
Product code
Code EZL
Device class
Class 2
Regulation
21 CFR 876.5130
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Emek Hayarden, IL
Download summary PDFView on FDA.gov ↗

Recent devices under product code EZL

view all

More clearances from Degania Silicone , Ltd.

view all

Adverse events under product code EZL

product code EZL
Death
6
Injury
796
Malfunction
4,989
Other
1
Total
5,792

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 K063442

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 K063442.

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