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FDA 510(k)

DESERET SUBCLAVIAN JUGULAR CATH-SET

K-Number: K833091 · 1983-11-21

ApplicantWarner-Lambert Co.
Decision Date1983-11-21
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET SUBCLAVIAN JUGULAR CATH-SET 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 K833091. 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 SUBCLAVIAN JUGULAR CATH-SET?

DESERET SUBCLAVIAN JUGULAR CATH-SET 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 K833091.

When did DESERET SUBCLAVIAN JUGULAR CATH-SET receive FDA 510(k) clearance?

DESERET SUBCLAVIAN JUGULAR CATH-SET received FDA 510(k) clearance on 1983-11-21, under 510(k) number K833091.

Who is the listed applicant for DESERET SUBCLAVIAN JUGULAR CATH-SET?

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 SUBCLAVIAN JUGULAR CATH-SET?

The FDA product code for DESERET SUBCLAVIAN JUGULAR CATH-SET is FOZ.

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Other records listing Warner-Lambert Co. as applicant

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Related Devices (Code: 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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