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FDA 510(k)

SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME

K-Number: K896466 · 1990-02-08

Decision Date1990-02-08
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME 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 1990-02-08 under 510(k) number K896466. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME?

SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME is a medical device that received FDA 510(k) clearance on 1990-02-08. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K896466.

When did SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME receive FDA 510(k) clearance?

SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME received FDA 510(k) clearance on 1990-02-08, under 510(k) number K896466.

Who is the listed applicant for SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME?

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 SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME?

The FDA product code for SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME is DYG.

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.

Other records listing Baxter Healthcare 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.

View all 504 devices →

Related Devices (Code: DYG)

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.

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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