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FDA 510(k)

ITC ANGIOGRAPHIC CATHETER

K-Number: K900757 · 1990-08-14

ApplicantInterventional Therapeutics Corp.
Decision Date1990-08-14
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ITC ANGIOGRAPHIC CATHETER 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 1990-08-14 under 510(k) number K900757. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITC ANGIOGRAPHIC CATHETER?

ITC ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K900757.

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

ITC ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1990-08-14, under 510(k) number K900757.

Who is the listed applicant for ITC ANGIOGRAPHIC CATHETER?

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 ITC ANGIOGRAPHIC CATHETER?

The FDA product code for ITC ANGIOGRAPHIC CATHETER is DQA.

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Other records listing Interventional Therapeutics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960832OCCLUSION BALLOON CATHETERK950398CATHETER, BALLOON TYPEK945588DISPOSABLE 1CC SYRINGE WITH LUER LOCKK944354CONTOUR EMBOLIK930456INTHERM SINGLE-STICK RADIALLY EXPANDING DILATORK914866ITC CONTOUR EMBOLI, MODIFICATION

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Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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