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

URESIL DILATOR WITH RADIOPAQUE MARKER

K Number: K980282 · Decision Apr 24, 1998
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
103
Applicant Total
45
Review Days
88

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Basic Information

Device Name
URESIL DILATOR WITH RADIOPAQUE MARKER
K Number
K980282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Uresil Corp.
Date Received
January 26, 1998
Decision Date
April 24, 1998
Product Code
DRE
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
DRE Dilator, Vessel, For Percutaneous Catheterization

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K953923 URESIL INTRODUCING NEEDLE
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