FDA 510(k)

SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER

K-Number: K915351 · 1992-06-29

ApplicantMedtronics Interventional Vascular

Decision Date1992-06-29

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER 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 1992-06-29 under 510(k) number K915351. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER?

SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER is a medical device that received FDA 510(k) clearance on 1992-06-29. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K915351.

When did SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER receive FDA 510(k) clearance?

SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER received FDA 510(k) clearance on 1992-06-29, under 510(k) number K915351.

Who is the listed applicant for SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER?

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 SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER?

The FDA product code for SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER is DQO.

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Official Source

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