ROSS ENTERAL FEEDING TUBE
K-Number: K972437 · 1998-01-26
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Device Summary
Frequently Asked Questions
What is the ROSS ENTERAL FEEDING TUBE?
ROSS ENTERAL FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1998-01-26. The listed applicant is Ross Products. The 510(k) number is K972437.
When did ROSS ENTERAL FEEDING TUBE receive FDA 510(k) clearance?
ROSS ENTERAL FEEDING TUBE received FDA 510(k) clearance on 1998-01-26, under 510(k) number K972437.
Who is the listed applicant for ROSS ENTERAL FEEDING TUBE?
The FDA 510(k) record lists Ross Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROSS ENTERAL FEEDING TUBE?
The FDA product code for ROSS 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 Ross Products 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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