ENTERNAL FEEDING TUBE-POLYURETHANE EF504
K-Number: K844175 · 1985-01-02
Advertisement
Device Summary
Frequently Asked Questions
What is the ENTERNAL FEEDING TUBE-POLYURETHANE EF504?
ENTERNAL FEEDING TUBE-POLYURETHANE EF504 is a medical device that received FDA 510(k) clearance on 1985-01-02. The listed applicant is Exco, Inc.. The 510(k) number is K844175.
When did ENTERNAL FEEDING TUBE-POLYURETHANE EF504 receive FDA 510(k) clearance?
ENTERNAL FEEDING TUBE-POLYURETHANE EF504 received FDA 510(k) clearance on 1985-01-02, under 510(k) number K844175.
Who is the listed applicant for ENTERNAL FEEDING TUBE-POLYURETHANE EF504?
The FDA 510(k) record lists Exco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERNAL FEEDING TUBE-POLYURETHANE EF504?
The FDA product code for ENTERNAL FEEDING TUBE-POLYURETHANE EF504 is KNT.
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 Exco, 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: KNT)
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.
Advertisement