Cleared Traditional

K852300 - INOX IV STAND

K852300 is an FDA 510(k) clearance for INOX IV STAND, manufactured by Broadwest Corp.. The device is a Class 1 General Hospital device with product code FOX cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K852300 · Broadwest Corp. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1985
Decision
22d
Days
Class 1
Risk

K852300 is an FDA 510(k) clearance for the INOX IV STAND. Classified as Stand, Infusion (product code FOX), Class I - General Controls.

Submitted by Broadwest Corp. (New York, US). The FDA issued a Cleared decision on June 20, 1985 after a review of 22 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 Broadwest Corp. devices

FDA 510(k) Submission Details - K852300

510(k) Number K852300 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 29, 1985
Decision Date June 20, 1985
Days to Decision 22 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
107d faster than avg
Panel avg: 129d · This submission: 22d
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 K852300.
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