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

INTERMITTENT URETHRAL CATHETERS

K Number: K033023 · Decision Dec 23, 2003
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
43
Review Days
88

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Basic Information

Device Name
INTERMITTENT URETHRAL CATHETERS
K Number
K033023
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
September 26, 2003
Decision Date
December 23, 2003
Product Code
KOD
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
KOD Catheter, Urological

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Other Clearances by Rusch Intl.

K Number Device Name
K030559 RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEM
K023666 RUSCH GUIDED CHOLANGIOGRAPHY CATHETER
K023918 RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESS
K023964 RUSCH MICROLARYNGEAL TUBE
K021540 RUSCH EDGAR TUBE
K021764 RUSCH TRACHEOFIX SET, CUFFED AND UNCUFFED
K020714 RUSCH FLONEIL; FLOCATH INTROGEL
K010798 RUSCH CANTOR TUBE
K010797 RUSCH MILLER-ABBOTT TUBE
K013872 RUSCH MEMORY BAG
Search all 43 clearances from Rusch Intl. →