FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

HI TORQUE CONNECT GUIDEWIRE

K Number: K112381 · Decision Nov 3, 2011
Classifications
1
FEI Numbers
252
Registration Numbers
253
Same Product Code
751
Applicant Total
10
Review Days
78

Basic Information

Device Name
HI TORQUE CONNECT GUIDEWIRE
K Number
K112381
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LAKE REGION MEDICAL
Date Received
August 17, 2011
Decision Date
November 3, 2011
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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