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FDA 510(k)

DESERET SUBCLAVIAN JUGULAR CATHETER SET

K-Number: K821699 · 1982-06-24

ApplicantWarner-Lambert Co.
Decision Date1982-06-24
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET SUBCLAVIAN JUGULAR CATHETER 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 1982-06-24 under 510(k) number K821699. 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 CATHETER SET?

DESERET SUBCLAVIAN JUGULAR CATHETER SET is a medical device that received FDA 510(k) clearance on 1982-06-24. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821699.

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

DESERET SUBCLAVIAN JUGULAR CATHETER SET received FDA 510(k) clearance on 1982-06-24, under 510(k) number K821699.

Who is the listed applicant for DESERET SUBCLAVIAN JUGULAR CATHETER 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 CATHETER SET?

The FDA product code for DESERET SUBCLAVIAN JUGULAR CATHETER 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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