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FDA 510(k)

ITC CONTOUR EMBOLI, MODIFICATION

K-Number: K914866 · 1993-11-09

ApplicantInterventional Therapeutics Corp.
Decision Date1993-11-09
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ITC CONTOUR EMBOLI, 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 1993-11-09 under 510(k) number K914866. 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 CONTOUR EMBOLI, MODIFICATION?

ITC CONTOUR EMBOLI, MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-11-09. The listed applicant is Interventional Therapeutics Corp.. The 510(k) number is K914866.

When did ITC CONTOUR EMBOLI, MODIFICATION receive FDA 510(k) clearance?

ITC CONTOUR EMBOLI, MODIFICATION received FDA 510(k) clearance on 1993-11-09, under 510(k) number K914866.

Who is the listed applicant for ITC CONTOUR EMBOLI, 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 ITC CONTOUR EMBOLI, MODIFICATION?

The FDA product code for ITC CONTOUR EMBOLI, MODIFICATION is HCG.

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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.

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Related Devices (Code: HCG)

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.

K262419MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MFCerenovus, Inc.K261772Target Xtra Detachable CoilStryker NeurovscularK260351Numen™ Helia Coil Embolization System; NumenFR™ Detachment SystemMicroPort NeuroTech (Shanghai) Co., Ltd.K254221Optima Coil System (OptiOne Coil System)Balt USA, LLCK252694Target Detachable CoilStryker NeurovascularK251832InZone IST Detachment System; IZDS Connecting CableStryker Neurovascular

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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