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FDA 510(k)

FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70

K-Number: K955525 · 1996-08-08

ApplicantInterventional Innovations Corp.
Decision Date1996-08-08
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 is the device name listed in this FDA 510(k) record. The listed applicant is Interventional Innovations Corp.. It received FDA 510(k) clearance on 1996-08-08 under 510(k) number K955525. 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 FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70?

FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 is a medical device that received FDA 510(k) clearance on 1996-08-08. The listed applicant is Interventional Innovations Corp.. The 510(k) number is K955525.

When did FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 receive FDA 510(k) clearance?

FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 received FDA 510(k) clearance on 1996-08-08, under 510(k) number K955525.

Who is the listed applicant for FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70?

The FDA 510(k) record lists Interventional Innovations Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70?

The FDA product code for FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 is KRA.

Related Clinical Trials

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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Other records listing Interventional Innovations 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.

K964154SEGUE INFUSION CATHETER

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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