FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Rüsch Latex Gold Foley Catheter

K Number: K232469 · Decision Aug 1, 2024
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
64
Review Days
352

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Basic Information

Device Name
Rüsch Latex Gold Foley Catheter
K Number
K232469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teleflexmedical, Inc.
Date Received
August 15, 2023
Decision Date
August 1, 2024
Product Code
EZL
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EZL Catheter, Retention Type, Balloon

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