PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907
K-Number: K050777 · 2005-04-22
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Device Summary
Frequently Asked Questions
What is the PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907?
PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907 is a medical device that received FDA 510(k) clearance on 2005-04-22. The listed applicant is Conmedcorp. The 510(k) number is K050777.
When did PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907 receive FDA 510(k) clearance?
PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907 received FDA 510(k) clearance on 2005-04-22, under 510(k) number K050777.
Who is the listed applicant for PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907?
The FDA 510(k) record lists Conmedcorp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907?
The FDA product code for PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907 is FGE.
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 Conmedcorp 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: FGE)
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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