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

INTRODUCER WITH DISTAL RADIOPAQUE MARKER BAND, MODEL OR-4926XX

K Number: K002847 · Decision May 31, 2001
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
26
Review Days
260

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Basic Information

Device Name
INTRODUCER WITH DISTAL RADIOPAQUE MARKER BAND, MODEL OR-4926XX
K Number
K002847
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Maxxim Medical
Date Received
September 13, 2000
Decision Date
May 31, 2001
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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