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

EXPANDABLE BILIARY STENT ENDOPROSTHESIS

K Number: K885180 · Decision Feb 16, 1989
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
22
Review Days
64

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Basic Information

Device Name
EXPANDABLE BILIARY STENT ENDOPROSTHESIS
K Number
K885180
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Schneider Intl., Ltd.
Date Received
December 14, 1988
Decision Date
February 16, 1989
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

Similar 510(k) Clearances

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Other Clearances by Schneider Intl., Ltd.

K Number Device Name
K925406 BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM
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
Search all 22 clearances from Schneider Intl., Ltd. →