ROSS EMBRACE ENTERAL PUMP
K-Number: K031407 · 2003-05-20
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Device Summary
Frequently Asked Questions
What is the ROSS EMBRACE ENTERAL PUMP?
ROSS EMBRACE ENTERAL PUMP is a medical device that received FDA 510(k) clearance on 2003-05-20. The listed applicant is Ross Product Div. Abbott Laboratories. The 510(k) number is K031407.
When did ROSS EMBRACE ENTERAL PUMP receive FDA 510(k) clearance?
ROSS EMBRACE ENTERAL PUMP received FDA 510(k) clearance on 2003-05-20, under 510(k) number K031407.
Who is the listed applicant for ROSS EMBRACE ENTERAL PUMP?
The FDA 510(k) record lists Ross Product Div. Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROSS EMBRACE ENTERAL PUMP?
The FDA product code for ROSS EMBRACE ENTERAL PUMP is LZH.
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 Product Div. Abbott Laboratories 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: LZH)
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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