FDA 510(k)

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE

K-Number: K925342 · 1993-05-06

ApplicantMedtronics Interventional Vascular

Decision Date1993-05-06

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE 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 1993-05-06 under 510(k) number K925342. 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 INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE?

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1993-05-06. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K925342.

When did MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE receive FDA 510(k) clearance?

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE received FDA 510(k) clearance on 1993-05-06, under 510(k) number K925342.

Who is the listed applicant for MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE?

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 INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE?

The FDA product code for MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE 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.