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FDA 510(k)

ITC INTRODUCER CATHETER

K-Number: K900756 · 1990-08-08

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

Device Summary

ITC INTRODUCER 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 1990-08-08 under 510(k) number K900756. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITC INTRODUCER CATHETER?

ITC INTRODUCER CATHETER is a medical device that received FDA 510(k) clearance on 1990-08-08. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K900756.

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

ITC INTRODUCER CATHETER received FDA 510(k) clearance on 1990-08-08, under 510(k) number K900756.

Who is the listed applicant for ITC INTRODUCER 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 INTRODUCER CATHETER?

The FDA product code for ITC INTRODUCER CATHETER is DYB.

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Other records listing Interventional Therapeutics Corp. as applicant

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Related Devices (Code: DYB)

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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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