Infant Feeding Tube

FDA 510(k) K042112 · Marian Medical, Inc.

Substantially Equivalent

510(k) numberK042112

Submission

Device name
Infant Feeding Tube
Applicant
Marian Medical, Inc.
Destin, FL, US
Received
August 5, 2004
Decision date
January 28, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Tube cleared by the FDA?

Infant Feeding Tube (K042112) received a 510(k) decision of Substantially Equivalent on January 28, 2005, 176 days after the submission was received.

What is the product code of K042112?

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