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FDA 510(k)

DESERET MULTILUMEN SUBCLAVIAN JUGULAR

K-Number: K840183 · 1984-03-19

ApplicantParke-Davis Co.
Decision Date1984-03-19
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET MULTILUMEN SUBCLAVIAN JUGULAR is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840183. 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 MULTILUMEN SUBCLAVIAN JUGULAR?

DESERET MULTILUMEN SUBCLAVIAN JUGULAR is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Parke-Davis Co.. The 510(k) number is K840183.

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

DESERET MULTILUMEN SUBCLAVIAN JUGULAR received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840183.

Who is the listed applicant for DESERET MULTILUMEN SUBCLAVIAN JUGULAR?

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

What is the FDA product code for DESERET MULTILUMEN SUBCLAVIAN JUGULAR?

The FDA product code for DESERET MULTILUMEN SUBCLAVIAN JUGULAR is FOZ.

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Other records listing Parke-Davis 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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