Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BARD CATH LAB THERMODILUTION CATHETER

K-Number: K893474 · 1989-09-05

Decision Date1989-09-05
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD CATH LAB THERMODILUTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1989-09-05 under 510(k) number K893474. 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 BARD CATH LAB THERMODILUTION CATHETER?

BARD CATH LAB THERMODILUTION CATHETER is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K893474.

When did BARD CATH LAB THERMODILUTION CATHETER receive FDA 510(k) clearance?

BARD CATH LAB THERMODILUTION CATHETER received FDA 510(k) clearance on 1989-09-05, under 510(k) number K893474.

Who is the listed applicant for BARD CATH LAB THERMODILUTION CATHETER?

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

What is the FDA product code for BARD CATH LAB THERMODILUTION CATHETER?

The FDA product code for BARD CATH LAB THERMODILUTION CATHETER 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 C.R. Bard, 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.

View all 616 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑