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

RUSCH INTERNATIONAL URODYNAMIC CATHETERS

K Number: K952029 · Decision Jun 13, 1995
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
35
Applicant Total
43
Review Days
43

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Basic Information

Device Name
RUSCH INTERNATIONAL URODYNAMIC CATHETERS
K Number
K952029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1620
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
May 1, 1995
Decision Date
June 13, 1995
Product Code
FEN
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
FEN Device, Cystometric, Hydraulic

Similar 510(k) Clearances

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Other Clearances by Rusch Intl.

K Number Device Name
K033023 INTERMITTENT URETHRAL CATHETERS
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
Search all 43 clearances from Rusch Intl. →