Hospira Enteral Feeding Set, Model 20640

FDA 510(k) K061432 · Hospira, Inc.

Substantially Equivalent

510(k) numberK061432

Submission

Device name
Hospira Enteral Feeding Set, Model 20640
Applicant
Hospira, Inc.
Lake Forest, IL, US
Received
May 24, 2006
Decision date
September 11, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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Questions and answers

When was Hospira Enteral Feeding Set, Model 20640 cleared by the FDA?

Hospira Enteral Feeding Set, Model 20640 (K061432) received a 510(k) decision of Substantially Equivalent on September 11, 2006, 110 days after the submission was received.

What is the product code of K061432?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.