Infant Feeding Tube

FDA 510(k) K896559 · Westmark, Sterile Packing Systems, Inc. (Sps)

Substantially Equivalent

510(k) numberK896559

Submission

Device name
Infant Feeding Tube
Applicant
Westmark, Sterile Packing Systems, Inc. (Sps)
Grand Rapids, MI, US
Received
November 17, 1989
Decision date
March 13, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPD – Tube, Feeding
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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More from Philips Children'S Medical Ventures

510(k)DeviceDecision
K896800Irrigation TrayKYZ · Traditional 05/24/1990SESK
K896799Paracervical/Pudendal TraysCAZ · Traditional 04/23/1990SE
K896794Specimen ContainerLIO · Traditional 03/01/1990SE
K896806Catheter Plug/ProtectorKNY · Traditional 02/26/1990SE
K896798Tracheostomy TrayBTO · Traditional 02/22/1990SE
K896797Suction Catheter KitBSY · Traditional 02/16/1990SE
K896215Mercy Hip/Knee PackKKX · Traditional 02/13/1990SE
K896804ManifoldGCX · Traditional 02/08/1990SE
K896563Tubing ConnectorsGCX · Traditional 02/06/1990SE
K896562StopcockGCX · Traditional 02/06/1990SE

Questions and answers

When was Infant Feeding Tube cleared by the FDA?

Infant Feeding Tube (K896559) received a 510(k) decision of Substantially Equivalent on March 13, 1990, 116 days after the submission was received.

What is the product code of K896559?

The FDA product code is FPD – Tube, Feeding, a Class II (moderate risk) device regulated under 21 CFR 876.5980.