FDA 510(k)

DESERET ANGIO-GUIDE LARGE VEIN CATH.

K-Number: K833092 · 1983-11-21

Decision Date1983-11-21

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DESERET ANGIO-GUIDE LARGE VEIN CATH. 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 1983-11-21 under 510(k) number K833092. 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 LARGE VEIN CATH.?

DESERET ANGIO-GUIDE LARGE VEIN CATH. is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Warner-Lambert Co.. The 510(k) number is K833092.

When did DESERET ANGIO-GUIDE LARGE VEIN CATH. receive FDA 510(k) clearance?

DESERET ANGIO-GUIDE LARGE VEIN CATH. received FDA 510(k) clearance on 1983-11-21, under 510(k) number K833092.

Who is the listed applicant for DESERET ANGIO-GUIDE LARGE VEIN CATH.?

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 LARGE VEIN CATH.?

The FDA product code for DESERET ANGIO-GUIDE LARGE VEIN CATH. is FOZ.

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Other records listing Warner-Lambert Co. as applicant

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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.