FDA 510(k)

BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH

K-Number: K911367 · 1991-06-10

Decision Date1991-06-10

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1991-06-10 under 510(k) number K911367. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH?

BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH is a medical device that received FDA 510(k) clearance on 1991-06-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K911367.

When did BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH receive FDA 510(k) clearance?

BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH received FDA 510(k) clearance on 1991-06-10, under 510(k) number K911367.

Who is the listed applicant for BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH?

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

What is the FDA product code for BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH?

The FDA product code for BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH is DQO.

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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.