SWAN-GANZ FLOW-DIRECTED THERMODIL. CATH
K-Number: K822350 · 1982-08-24
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Device Summary
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.
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.
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