Cleared Traditional

K860468 - UNICADDY I & II I.V. CONTAINER CADDY IMS POLE MATE

K860468 is an FDA 510(k) clearance for UNICADDY I & II I.V. CONTAINER CADDY IM..., manufactured by Intl. Medication Systems, Ltd.. The device is a Class 1 General Hospital device with product code FOX cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K860468 · Intl. Medication Systems, Ltd. · General Hospital
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Mar 1986
Decision
40d
Days
Class 1
Risk

K860468 is an FDA 510(k) clearance for the UNICADDY I & II I.V. CONTAINER CADDY IMS POLE MATE. Classified as Stand, Infusion (product code FOX), Class I - General Controls.

Submitted by Intl. Medication Systems, Ltd. (South El Monte, US). The FDA issued a Cleared decision on March 18, 1986 after a review of 40 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6990 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Intl. Medication Systems, Ltd. devices

FDA 510(k) Submission Details - K860468

510(k) Number K860468 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 06, 1986
Decision Date March 18, 1986
Days to Decision 40 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
89d faster than avg
Panel avg: 129d · This submission: 40d
Pathway characteristics
Predicate-based equivalence.

FOX Device Classification - Class 1, General Controls

Product Code FOX Stand, Infusion
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6990
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FOX Stand, Infusion

All 11
Devices cleared under the same product code (FOX) and FDA review panel - the closest regulatory comparables to K860468.
HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER
K883133 · Ferguson Medical · Nov 1988
POLE, INTRAVENOUS
K880537 · Ferguson Medical · Apr 1988
TRACK AND CARRIER, INTRAVENOUS
K880538 · Ferguson Medical · Feb 1988
IMPACT 901 SERIES PORT-A-WALL
K850671 · Impact Instrumentation, Inc. · Mar 1985
CATHETER, SURFLO, I.V.
K770422 · Terumo America, Inc. · Mar 1977