FDA 510(k)

ITC BUNJI PLATINUM EMBOLIZATION COIL

K-Number: K925876 · 1993-04-15

ApplicantInterventional Therapeutics Corp.

Decision Date1993-04-15

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ITC BUNJI PLATINUM EMBOLIZATION COIL 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 1993-04-15 under 510(k) number K925876. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITC BUNJI PLATINUM EMBOLIZATION COIL?

ITC BUNJI PLATINUM EMBOLIZATION COIL is a medical device that received FDA 510(k) clearance on 1993-04-15. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K925876.

When did ITC BUNJI PLATINUM EMBOLIZATION COIL receive FDA 510(k) clearance?

ITC BUNJI PLATINUM EMBOLIZATION COIL received FDA 510(k) clearance on 1993-04-15, under 510(k) number K925876.

Who is the listed applicant for ITC BUNJI PLATINUM EMBOLIZATION COIL?

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 BUNJI PLATINUM EMBOLIZATION COIL?

The FDA product code for ITC BUNJI PLATINUM EMBOLIZATION COIL is HCG.

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Other records listing Interventional Therapeutics Corp. as applicant

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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.