FDA 510(k)

HIGH PRESSURE CONTRAST INJECTION LINE

K-Number: K822100 · 1982-08-24

ApplicantNamic

Decision Date1982-08-24

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HIGH PRESSURE CONTRAST INJECTION LINE is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1982-08-24 under 510(k) number K822100. 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 HIGH PRESSURE CONTRAST INJECTION LINE?

HIGH PRESSURE CONTRAST INJECTION LINE is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is Namic. The 510(k) number is K822100.

When did HIGH PRESSURE CONTRAST INJECTION LINE receive FDA 510(k) clearance?

HIGH PRESSURE CONTRAST INJECTION LINE received FDA 510(k) clearance on 1982-08-24, under 510(k) number K822100.

Who is the listed applicant for HIGH PRESSURE CONTRAST INJECTION LINE?

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 HIGH PRESSURE CONTRAST INJECTION LINE?

The FDA product code for HIGH PRESSURE CONTRAST INJECTION LINE 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.