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

Hi-Torque Command 18 Guide Wire

K Number: K152404 · Decision Sep 21, 2015
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
30
Review Days
27

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Basic Information

Device Name
Hi-Torque Command 18 Guide Wire
K Number
K152404
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Vascular
Date Received
August 25, 2015
Decision Date
September 21, 2015
Product Code
DQX
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
DQX Wire, Guide, Catheter

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