FDA 510(k)

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)

K-Number: K960801 · 1996-03-29

ApplicantNorth American Instrument Corp.

Decision Date1996-03-29

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) 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 1996-03-29 under 510(k) number K960801. 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 SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)?

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is North American Instrument Corp.. The 510(k) number is K960801.

When did SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) receive FDA 510(k) clearance?

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) received FDA 510(k) clearance on 1996-03-29, under 510(k) number K960801.

Who is the listed applicant for SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)?

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 SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)?

The FDA product code for SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) 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.