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

ERCP CANNULA

K Number: K905714 · Decision Feb 1, 1991
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
21
Review Days
42

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Basic Information

Device Name
ERCP CANNULA
K Number
K905714
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Everest Medical Corp.
Date Received
December 21, 1990
Decision Date
February 1, 1991
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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K955001 EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS
K945975 EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS
K922509 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA
K922246 TUBING SET W/ IRRIGATION & ASPIRATION VALVING
K920089 MONOPOLAR COAGULATING POLYPECTOMY SNARE
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