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)

SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH

K-Number: K822350 · 1982-08-24

Decision Date1982-08-24
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH is the device name listed in this FDA 510(k) record. The listed applicant is American Edwards Laboratories. It received FDA 510(k) clearance on 1982-08-24 under 510(k) number K822350. 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 FLOW-DIRECTED THERMODIL. CATH?

SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is American Edwards Laboratories. The 510(k) number is K822350.

When did SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH receive FDA 510(k) clearance?

SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH received FDA 510(k) clearance on 1982-08-24, under 510(k) number K822350.

Who is the listed applicant for SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH?

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

What is the FDA product code for SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH?

The FDA product code for SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH 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 American Edwards Laboratories 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 89 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.

↑