Infant Feeding Tubes

FDA 510(k) K020005 · Promedic, Inc.

Substantially Equivalent

510(k) numberK020005

Submission

Device name
Infant Feeding Tubes
Applicant
Promedic, Inc.
Mccordsville, IN, US
Received
January 2, 2002
Decision date
July 16, 2002
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 Infant Feeding Tubes cleared by the FDA?

Infant Feeding Tubes (K020005) received a 510(k) decision of Substantially Equivalent on July 16, 2002, 195 days after the submission was received.

What is the product code of K020005?

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