Empty Solution Transfer Container

FDA 510(k) K842170 · The Healthcare Group Laboratories, Inc.

Substantially Equivalent

510(k) numberK842170

Submission

Device name
Empty Solution Transfer Container
Applicant
The Healthcare Group Laboratories, Inc.
Orem, UT, US
Received
May 24, 1984
Decision date
October 19, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KPE – Container, I.V.
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5025
Specialty
General Hospital

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More from Gilero, LLC

510(k)DeviceDecision
K850035Empty Solution Transfer ContainerKPE · Traditional 06/07/1985SE
K842091Dispos. Acu-Cut Soft Tissue Biopsy · Traditional 07/23/1984SE
K840742Right Atrial CatheterLJS · Traditional 07/13/1984SE
K830299Solution Transfer ContainerKPE · Traditional 02/19/1983SE
K822307Adhesive Spray #4050-4060KNX · Traditional 09/24/1982SE
K822059Show'RbagLGF · Traditional 07/22/1982SE
K821480Right Atrial Catheters Parenteral NutritDQY · Traditional 06/17/1982SE
K821230Softic 49EBI · Traditional 05/28/1982SE
K821162Adhesive RemoverKOX · Traditional 05/14/1982SE
K821172External Female Urinary IncontinenceKNX · Traditional 05/10/1982SE

Questions and answers

When was Empty Solution Transfer Container cleared by the FDA?

Empty Solution Transfer Container (K842170) received a 510(k) decision of Substantially Equivalent on October 19, 1984, 148 days after the submission was received.

What is the product code of K842170?

The FDA product code is KPE – Container, I.V., a Class II (moderate risk) device regulated under 21 CFR 880.5025.