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)

THERMAL DILUTION CATHETER

K-Number: K843411 · 1984-10-18

Decision Date1984-10-18
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THERMAL DILUTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Andover Medical, Inc.. It received FDA 510(k) clearance on 1984-10-18 under 510(k) number K843411. 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 THERMAL DILUTION CATHETER?

THERMAL DILUTION CATHETER is a medical device that received FDA 510(k) clearance on 1984-10-18. The listed applicant is Andover Medical, Inc.. The 510(k) number is K843411.

When did THERMAL DILUTION CATHETER receive FDA 510(k) clearance?

THERMAL DILUTION CATHETER received FDA 510(k) clearance on 1984-10-18, under 510(k) number K843411.

Who is the listed applicant for THERMAL DILUTION CATHETER?

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

What is the FDA product code for THERMAL DILUTION CATHETER?

The FDA product code for THERMAL DILUTION 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 Andover Medical, 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 21 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.

↑