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

MODEL SP5800 #8 FRENCH INTRO. KIT

K Number: K823262 · Decision Jan 18, 1983
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
31
Review Days
77

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Basic Information

Device Name
MODEL SP5800 #8 FRENCH INTRO. KIT
K Number
K823262
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Gould, Inc.
Date Received
November 2, 1982
Decision Date
January 18, 1983
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DYB Introducer, Catheter

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