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

AMERICAN CATHETER E.R.C.P. CANNULA

K Number: K940370 · Decision Aug 17, 1994
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
17
Review Days
203

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Basic Information

Device Name
AMERICAN CATHETER E.R.C.P. CANNULA
K Number
K940370
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intl. Medical, Inc.
Date Received
January 26, 1994
Decision Date
August 17, 1994
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 Intl. Medical, Inc.

K Number Device Name
K970507 PEAK FLOW METER
K943078 HOT BIOPSY FORCEPS
K940335 AMERICAN CATHETER POLY-SNARE
K942068 AMERICAN CATHETER SPHINCTEROTOME
K930406 DURHAM; MIN BORE LUER LOCK EXTENSION SET
K930410 DURHAM; LUER LOCK EXTENSION SET
K923200 AMCATH DISPOSABLE CYTOLOGY BRUSH
K915142 AMCATH DISPOSABLE BIOPSY FORCEPS
K912927 AMCATH DISPOSABLE TROCAR AND TROCAR SLEEVE
K912605 AMCATH DISPOSABLE MICRO SCISSORS
Search all 17 clearances from Intl. Medical, Inc. →