FDA Product Code KPE: Container, I.v.
Under FDA product code KPE, intravenous fluid containers are cleared for the storage and delivery of sterile IV solutions.
These flexible plastic bags or rigid bottles contain sterile isotonic, hypertonic, or hypotonic solutions — including saline, dextrose, and lactated Ringer's — for intravenous fluid and electrolyte replacement. They are a fundamental component of fluid therapy across all clinical settings.
KPE devices are Class II medical devices, regulated under 21 CFR 880.5025 and reviewed by the FDA General Hospital panel.
Leading manufacturers include Baxter Healthcare Corp, Abbott Laboratories and The Healthcare Group Laboratories, Inc..
117
Total
117
Cleared
108d
Avg days
1976
Since
117 devices
Cleared
Feb 19, 1983
SOLUTION TRANSFER CONTAINER
The Healthcare Group Laboratories, Inc.
General Hospital
22d
Cleared
Aug 27, 1980
TOTAL PARENTERAL NUTRITION SET BAG
Cutter Laboratories, Inc.
General Hospital
40d
Cleared
Oct 26, 1979
LIFE CARE 1000ML.EMP. CONT. W/AT. Y-TRAN
Abbott Laboratories
General Hospital
46d
Cleared
Oct 01, 1979
ADDITIVE HINGE CAP
Abbott Laboratories
Chemistry
17d
Cleared
Jun 01, 1979
CAP, TAMPER PROOF PLASTIC
Acacia, Inc.
General Hospital
164d
Cleared
Sep 28, 1977
HICALIQ IVH BAG
Terumo America, Inc.
General Hospital
58d
Cleared
Aug 02, 1977
LIFECARE EMPTY CONTAINER
Abbott Laboratories
General Hospital
26d
Cleared
Dec 30, 1976
ADDITIVE CAP (2B8905)
Travenol Laboratories, S.A.
General Hospital
70d