CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR
K-Number: K925444 · 1993-07-19
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Device Summary
Frequently Asked Questions
What is the CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR?
CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR is a medical device that received FDA 510(k) clearance on 1993-07-19. The listed applicant is Ami-Med Corp.. The 510(k) number is K925444.
When did CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR receive FDA 510(k) clearance?
CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR received FDA 510(k) clearance on 1993-07-19, under 510(k) number K925444.
Who is the listed applicant for CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR?
The FDA 510(k) record lists Ami-Med Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR?
The FDA product code for CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR 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.
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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