FDA 510(k)

NAMIC ANGIOGRAPHIC SYRINGE

K-Number: K873955 · 1988-02-05

ApplicantNorth American Instrument Corp.

Decision Date1988-02-05

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

NAMIC ANGIOGRAPHIC SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1988-02-05 under 510(k) number K873955. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMIC ANGIOGRAPHIC SYRINGE?

NAMIC ANGIOGRAPHIC SYRINGE is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is North American Instrument Corp.. The 510(k) number is K873955.

When did NAMIC ANGIOGRAPHIC SYRINGE receive FDA 510(k) clearance?

NAMIC ANGIOGRAPHIC SYRINGE received FDA 510(k) clearance on 1988-02-05, under 510(k) number K873955.

Who is the listed applicant for NAMIC ANGIOGRAPHIC SYRINGE?

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

What is the FDA product code for NAMIC ANGIOGRAPHIC SYRINGE?

The FDA product code for NAMIC ANGIOGRAPHIC SYRINGE is DXT.

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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.