HI-TORQUE POWERTURN

Wire, Guide, Catheter

ABBOTT VASCULAR-CARDIAC THERAPIES

The following data is part of a premarket notification filed by Abbott Vascular-cardiac Therapies with the FDA for Hi-torque Powerturn.

Pre-market Notification Details

Device IDK112957
510k NumberK112957
Device Name:HI-TORQUE POWERTURN
ClassificationWire, Guide, Catheter
Applicant ABBOTT VASCULAR-CARDIAC THERAPIES 26531 YNEZ RD. MAILING P.O. BOX 9018 Temecula,  CA  92589 -9018
ContactKay Setzer
CorrespondentKay Setzer
ABBOTT VASCULAR-CARDIAC THERAPIES 26531 YNEZ RD. MAILING P.O. BOX 9018 Temecula,  CA  92589 -9018
Product CodeDQX  
CFR Regulation Number870.1330 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-10-04
Decision Date2011-11-08
Summary:summary

Trademark Results [HI-TORQUE POWERTURN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HI-TORQUE POWERTURN
HI-TORQUE POWERTURN
87937200 5771180 Live/Registered
Abbott Cardiovascular Systems Inc.
2018-05-25
HI-TORQUE POWERTURN
HI-TORQUE POWERTURN
85285224 not registered Dead/Abandoned
Abbott Cardiovascular Systems Inc.
2011-04-04

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