FDA 510(k)

DESERET GUIDEWIRE INTRODUCER II

K-Number: K920407 · 1992-04-07

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1992-04-07

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DESERET GUIDEWIRE INTRODUCER II is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1992-04-07 under 510(k) number K920407. 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 DESERET GUIDEWIRE INTRODUCER II?

DESERET GUIDEWIRE INTRODUCER II is a medical device that received FDA 510(k) clearance on 1992-04-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K920407.

When did DESERET GUIDEWIRE INTRODUCER II receive FDA 510(k) clearance?

DESERET GUIDEWIRE INTRODUCER II received FDA 510(k) clearance on 1992-04-07, under 510(k) number K920407.

Who is the listed applicant for DESERET GUIDEWIRE INTRODUCER II?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET GUIDEWIRE INTRODUCER II?

The FDA product code for DESERET GUIDEWIRE INTRODUCER II 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.