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

CORDIS BRITE TIP SHEATH INTRODUCER

K Number: K954595 · Decision Dec 28, 1995
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
315
Review Days
86

Basic Information

Device Name
CORDIS BRITE TIP SHEATH INTRODUCER
K Number
K954595
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CORDIS CORP.
Date Received
October 3, 1995
Decision Date
December 28, 1995
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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