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FDA 510(k)

ITC GUIDING CATHETER

K-Number: K913052 · 1991-11-22

ApplicantInterventional Therapeutics Corp.
Decision Date1991-11-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ITC GUIDING 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 1991-11-22 under 510(k) number K913052. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITC GUIDING CATHETER?

ITC GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K913052.

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

ITC GUIDING CATHETER received FDA 510(k) clearance on 1991-11-22, under 510(k) number K913052.

Who is the listed applicant for ITC GUIDING 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 GUIDING CATHETER?

The FDA product code for ITC GUIDING CATHETER is DQY.

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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: DQY)

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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