FDA 510(k)

CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS)

K-Number: K960159 · 1996-10-25

Decision Date1996-10-25

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1996-10-25 under 510(k) number K960159. 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 CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS)?

CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) is a medical device that received FDA 510(k) clearance on 1996-10-25. The listed applicant is Cordis Corp.. The 510(k) number is K960159.

When did CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) receive FDA 510(k) clearance?

CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) received FDA 510(k) clearance on 1996-10-25, under 510(k) number K960159.

Who is the listed applicant for CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS)?

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

What is the FDA product code for CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS)?

The FDA product code for CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) is JXG.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: JXG)

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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.