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FDA 510(k)

DESERET SUBCLAVIAN JUGULAR CATH. SET

K-Number: K834227 · 1984-03-19

ApplicantParke-Davis Co.
Decision Date1984-03-19
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 Parke-Davis Co.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K834227. 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 1984-03-19. The listed applicant is Parke-Davis Co.. The 510(k) number is K834227.

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

DESERET SUBCLAVIAN JUGULAR CATH. SET received FDA 510(k) clearance on 1984-03-19, under 510(k) number K834227.

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

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 SUBCLAVIAN JUGULAR CATH. SET?

The FDA product code for DESERET SUBCLAVIAN JUGULAR CATH. SET 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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