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

RUSCH SILICONE FOLEY CATHETER

K Number: K980870 · Decision Jun 9, 1998
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
26
Review Days
97

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Basic Information

Device Name
RUSCH SILICONE FOLEY CATHETER
K Number
K980870
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, Inc.
Date Received
March 4, 1998
Decision Date
June 9, 1998
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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Other Clearances by Rusch, Inc.

K Number Device Name
K010420 RUSCH MMG/O'NEIL CATHETER
K993528 RUSCH EMERGENCY MASK
K993194 RUSCH MANUAL RESUSCITATOR BAG
K974419 RUSCH SIMPLASTIC COUNCILL TIP CATHETER
K963779 RUSCH ENTERAL FEEDING TUBE
K970021 RUSCH SUPRAPUBIC TRAY
K963993 RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET
K955564 RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE
K955495 RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE
K953963 RUSCH SINGLE LUMEN BRONCHIAL TUVBE SET, STERILE, FOR LEFT & RIGHT SIDED BRONCHIAL INTUBATION
Search all 26 clearances from Rusch, Inc. →