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FDA 510(k)

1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS

K-Number: K983003 · 1998-09-17

ApplicantCordis Neurovascular, Inc.
Decision Date1998-09-17
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Neurovascular, Inc.. It received FDA 510(k) clearance on 1998-09-17 under 510(k) number K983003. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS?

1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS is a medical device that received FDA 510(k) clearance on 1998-09-17. The listed applicant is Cordis Neurovascular, Inc.. The 510(k) number is K983003.

When did 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS receive FDA 510(k) clearance?

1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS received FDA 510(k) clearance on 1998-09-17, under 510(k) number K983003.

Who is the listed applicant for 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS?

The FDA 510(k) record lists Cordis Neurovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS?

The FDA product code for 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS is KRA.

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Other records listing Cordis Neurovascular, Inc. as applicant

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Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

Official Source

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

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