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FDA 510(k)

TRI-FLOW CATHETER

K-Number: K875205 · 1988-05-31

ApplicantNeurodynamics, Inc.
Decision Date1988-05-31
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRI-FLOW CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Neurodynamics, Inc.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K875205. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI-FLOW CATHETER?

TRI-FLOW CATHETER is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Neurodynamics, Inc.. The 510(k) number is K875205.

When did TRI-FLOW CATHETER receive FDA 510(k) clearance?

TRI-FLOW CATHETER received FDA 510(k) clearance on 1988-05-31, under 510(k) number K875205.

Who is the listed applicant for TRI-FLOW CATHETER?

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

What is the FDA product code for TRI-FLOW CATHETER?

The FDA product code for TRI-FLOW CATHETER is JXG.

Related Clinical Trials

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Other records listing Neurodynamics, Inc. 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.

K932402MODIFICATION TO GHAJAR GUIDE TWIST DRILLK875018GHAJAR GUIDE TWIST DRILLK875019GHAJAR GUIDE SYSTEM FOR THE PERFORATOR

Related Devices (Code: JXG)

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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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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