Neonatal Feeding Kit

FDA 510(k) K864683 · Salt Creek Medical Technologies

Substantially Equivalent

510(k) numberK864683

Submission

Device name
Neonatal Feeding Kit
Applicant
Salt Creek Medical Technologies
Pinckney, MI, US
Received
December 2, 1986
Decision date
April 17, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Degania Silicone , Ltd.

510(k)DeviceDecision
K871042Urine Meter, 250CCKNX · Traditional 03/25/1987SE
K871087S.C.M.T. PerforatorHGE · Traditional 03/23/1987SE
K871075SCMT Umbilical ClampHFW · Traditional 03/23/1987SE
K864296S.C.T. Multi Port, Injection SiteFPA · Traditional 03/02/1987SE
K864682Salt Creek P.I. Tray · Traditional 01/06/1987SE
K864692Extension SetsFPK · Traditional 12/18/1986SE
K864693I.V. Start Kits · Traditional 12/16/1986SE

Questions and answers

When was Neonatal Feeding Kit cleared by the FDA?

Neonatal Feeding Kit (K864683) received a 510(k) decision of Substantially Equivalent on April 17, 1987, 136 days after the submission was received.

What is the product code of K864683?

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