RUSCH ENTERAL FEEDING TUBE
K-Number: K963779 · 1997-05-23
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Device Summary
Frequently Asked Questions
What is the RUSCH ENTERAL FEEDING TUBE?
RUSCH ENTERAL FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1997-05-23. The listed applicant is Rusch, Inc.. The 510(k) number is K963779.
When did RUSCH ENTERAL FEEDING TUBE receive FDA 510(k) clearance?
RUSCH ENTERAL FEEDING TUBE received FDA 510(k) clearance on 1997-05-23, under 510(k) number K963779.
Who is the listed applicant for RUSCH ENTERAL FEEDING TUBE?
The FDA 510(k) record lists Rusch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUSCH ENTERAL FEEDING TUBE?
The FDA product code for RUSCH 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 Rusch, Inc. 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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