FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ClaveQS™ Bag

K Number: K251980 · Decision Mar 20, 2026
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
66
Review Days
266

Basic Information

Device Name
ClaveQS™ Bag
K Number
K251980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icu Medical, Inc.
Date Received
June 27, 2025
Decision Date
March 20, 2026
Product Code
KPE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPE Container, I.V.

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPE), ordered by most recent decision date.

View all

Other Clearances by Icu Medical, Inc.

K Number Device Name
K252130 LifeShield Infusion Safety Software Suite
K252006 OTTO™ Disinfecting Cap
K250616 Clave™ Neutral-Displacement Needlefree Connectors
K242114 Plum Solo™ Precision IV Pump
K242117 LifeShield Infusion Safety Software Suite
K242115 Plum Duo™ Precision IV Pump
K243985 Rio™ Drug Reconstitution Transfer Device
K223607 Plum Duo™ Infusion System
K223606 LifeShield™ Infusion Safety Software Suite
K173477 ChemoCLAVE Cytotoxic Medication Preparation and Delivery System
Search all 66 clearances from Icu Medical, Inc. →