FDA 510(k)

ARTERIAL EXTENSION SET

K-Number: K790082 · 1979-01-25

ApplicantNamic

Decision Date1979-01-25

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ARTERIAL EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1979-01-25 under 510(k) number K790082. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL EXTENSION SET?

ARTERIAL EXTENSION SET is a medical device that received FDA 510(k) clearance on 1979-01-25. The listed applicant is Namic. The 510(k) number is K790082.

When did ARTERIAL EXTENSION SET receive FDA 510(k) clearance?

ARTERIAL EXTENSION SET received FDA 510(k) clearance on 1979-01-25, under 510(k) number K790082.

Who is the listed applicant for ARTERIAL EXTENSION SET?

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

What is the FDA product code for ARTERIAL EXTENSION SET?

The FDA product code for ARTERIAL EXTENSION SET is DQO.

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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.