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

BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM

K Number: K925406 · Decision Jan 11, 1995
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
22
Review Days
807

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Basic Information

Device Name
BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM
K Number
K925406
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Schneider Intl., Ltd.
Date Received
October 26, 1992
Decision Date
January 11, 1995
Product Code
FGE
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
FGE Stents, Drains And Dilators For The Biliary Ducts

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Other Clearances by Schneider Intl., Ltd.

K Number Device Name
K931577 SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI
K926271 SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO
K926003 SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETER
K925804 SCHNEIDER HYDRO-SIL GUIDEWIRE
K924591 SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER
K921856 TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.
K921943 SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BAL
K920157 SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETER
K915349 PTA BALLOON CATHETER
K914009 SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER
Search all 22 clearances from Schneider Intl., Ltd. →