FDA 510(k)

MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)

K-Number: K961917 · 1996-11-20

ApplicantMedtronics Interventional Vascular

Decision Date1996-11-20

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronics Interventional Vascular. It received FDA 510(k) clearance on 1996-11-20 under 510(k) number K961917. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)?

MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) is a medical device that received FDA 510(k) clearance on 1996-11-20. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K961917.

When did MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) receive FDA 510(k) clearance?

MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) received FDA 510(k) clearance on 1996-11-20, under 510(k) number K961917.

Who is the listed applicant for MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)?

The FDA 510(k) record lists Medtronics Interventional Vascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)?

The FDA product code for MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) is DQX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.