CORFLO ANTI IV ENTERAL FEEDING TUBE
K-Number: K083210 · 2008-12-29
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Device Summary
Frequently Asked Questions
What is the CORFLO ANTI IV ENTERAL FEEDING TUBE?
CORFLO ANTI IV ENTERAL FEEDING TUBE is a medical device that received FDA 510(k) clearance on 2008-12-29. The listed applicant is Corpak Medsystems. The 510(k) number is K083210.
When did CORFLO ANTI IV ENTERAL FEEDING TUBE receive FDA 510(k) clearance?
CORFLO ANTI IV ENTERAL FEEDING TUBE received FDA 510(k) clearance on 2008-12-29, under 510(k) number K083210.
Who is the listed applicant for CORFLO ANTI IV ENTERAL FEEDING TUBE?
The FDA 510(k) record lists Corpak Medsystems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORFLO ANTI IV ENTERAL FEEDING TUBE?
The FDA product code for CORFLO ANTI IV ENTERAL FEEDING TUBE is FPD.
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 Corpak Medsystems 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: FPD)
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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