FDA 510(k)

DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS

K-Number: K860867 · 1986-07-02

Decision Date1986-07-02

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1986-07-02 under 510(k) number K860867. 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 DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS?

DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS is a medical device that received FDA 510(k) clearance on 1986-07-02. The listed applicant is Medical Components, Inc.. The 510(k) number is K860867.

When did DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS receive FDA 510(k) clearance?

DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS received FDA 510(k) clearance on 1986-07-02, under 510(k) number K860867.

Who is the listed applicant for DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS?

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

What is the FDA product code for DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS?

The FDA product code for DIGITAL SUBTRACTION ANGIOGRAPHY CATHETERS AND SETS 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.