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

RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET

K Number: K963993 · Decision Dec 17, 1996
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
26
Review Days
74

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Basic Information

Device Name
RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET
K Number
K963993
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
October 4, 1996
Decision Date
December 17, 1996
Product Code
FCM
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
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

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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
K980870 RUSCH SILICONE FOLEY CATHETER
K974419 RUSCH SIMPLASTIC COUNCILL TIP CATHETER
K963779 RUSCH ENTERAL FEEDING TUBE
K970021 RUSCH SUPRAPUBIC TRAY
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. →