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

SINGLE LUMEN SUBCLAVIAN CANNULA

K Number: K840197 · Decision Apr 25, 1984
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
64
Applicant Total
174
Review Days
98

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Basic Information

Device Name
SINGLE LUMEN SUBCLAVIAN CANNULA
K Number
K840197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
January 18, 1984
Decision Date
April 25, 1984
Product Code
LFJ
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
LFJ Catheter, Subclavian

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