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FDA 510(k)

DESERET ANGIO GUIDE

K-Number: K821577 · 1982-06-16

ApplicantWarner-Lambert Co.
Decision Date1982-06-16
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET ANGIO GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-06-16 under 510(k) number K821577. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET ANGIO GUIDE?

DESERET ANGIO GUIDE is a medical device that received FDA 510(k) clearance on 1982-06-16. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821577.

When did DESERET ANGIO GUIDE receive FDA 510(k) clearance?

DESERET ANGIO GUIDE received FDA 510(k) clearance on 1982-06-16, under 510(k) number K821577.

Who is the listed applicant for DESERET ANGIO GUIDE?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET ANGIO GUIDE?

The FDA product code for DESERET ANGIO GUIDE is FOZ.

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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.

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