I.V. Start Kits

FDA 510(k) K864693 · Salt Creek Medical Technologies

Substantially Equivalent

510(k) numberK864693

Submission

Device name
I.V. Start Kits
Applicant
Salt Creek Medical Technologies
Canfield, OH, US
Received
December 2, 1986
Decision date
December 16, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Salt Creek Medical Technologies

510(k)DeviceDecision
K864683Neonatal Feeding KitKNT · Traditional 04/17/1987SE
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

Questions and answers

When was I.V. Start Kits cleared by the FDA?

I.V. Start Kits (K864693) received a 510(k) decision of Substantially Equivalent on December 16, 1986, 14 days after the submission was received.