FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

Coaxial Dilator Set (Micro-Introducer)

K Number: K172487 · Decision Oct 16, 2017
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
103
Applicant Total
14
Review Days
60

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Basic Information

Device Name
Coaxial Dilator Set (Micro-Introducer)
K Number
K172487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1310
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
Galt Medical Corp.
Date Received
August 17, 2017
Decision Date
October 16, 2017
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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K140028 GALT VTI LOW INSERTION VALVE TEARAWAY INTRODUCER
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K071330 GALTSTICK INTRODUCER SYSTEM
K043525 CATHETER INTRODUCER
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