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

UMI PERCUTANEOUS TRANSHEPATIC CHOLAN

K Number: K833937 · Decision Jan 3, 1984
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
21
Review Days
49

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Basic Information

Device Name
UMI PERCUTANEOUS TRANSHEPATIC CHOLAN
K Number
K833937
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Universal Medical Instrument Corp.
Date Received
November 15, 1983
Decision Date
January 3, 1984
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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K863178 UMI STEERABLE TORQUE GUIDE WIRE
K861984 UMI CATH-SEAL, 13+14F & TRANSSEPTAL CATHETER INTRO
K860168 UMI (FRANSEEN,WESTCOTT,GREENE,MENGHINI)BIO. NEEDLE
K851088 UMI ANGIOGRAPHIC CATHETER
K850820 PERCUTANEOUS CATHETER INTRODUCER W/CATH-SEAL & SID
K844558 UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE
Search all 21 clearances from Universal Medical Instrument Corp. →