FDA 510(k)

ANGIOGRAPHIC CATHETER -- MODIFICATION

K-Number: K922101 · 1993-02-12

ApplicantInterventional Therapeutics Corp.

Decision Date1993-02-12

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ANGIOGRAPHIC CATHETER -- MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Interventional Therapeutics Corp.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K922101. 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 ANGIOGRAPHIC CATHETER -- MODIFICATION?

ANGIOGRAPHIC CATHETER -- MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K922101.

When did ANGIOGRAPHIC CATHETER -- MODIFICATION receive FDA 510(k) clearance?

ANGIOGRAPHIC CATHETER -- MODIFICATION received FDA 510(k) clearance on 1993-02-12, under 510(k) number K922101.

Who is the listed applicant for ANGIOGRAPHIC CATHETER -- MODIFICATION?

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

What is the FDA product code for ANGIOGRAPHIC CATHETER -- MODIFICATION?

The FDA product code for ANGIOGRAPHIC CATHETER -- MODIFICATION 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.