Cleared Abbreviated

K140783 - HALO AMBULATORY INFUSION SYSTEM

K140783 is an FDA 510(k) clearance for HALO AMBULATORY INFUSION SYSTEM, manufactured by Zyno Medical, LLC. The device is a Class 2 General Hospital device with product code FRN cleared through the Abbreviated 510(k) pathway after a 200-day FDA review.

K140783 · Zyno Medical, LLC · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2014
Decision
200d
Days
Class 2
Risk

K140783 is an FDA 510(k) clearance for the HALO AMBULATORY INFUSION SYSTEM. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Zyno Medical, LLC (Natick, US). The FDA issued a Cleared decision on October 17, 2014 after a review of 200 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - the FDA general hospital device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Zyno Medical, LLC devices

FDA 510(k) Submission Details - K140783

510(k) Number K140783 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 2014
Decision Date October 17, 2014
Days to Decision 200 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d slower than avg
Panel avg: 129d · This submission: 200d
Pathway characteristics
Standards-based clearance path.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FRN Pump, Infusion

All 481
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K140783.
Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play Module
K161469 · Hospira, Inc. · Mar 2017
Infusomat Space Volumetric Infusion Pump
K142596 · B.Braun Medical, Inc. · Jun 2015
PLUM 360 INFUSION SYSTEM WITH HOSPIRA MEDNET, SMART CARD PLUG N PLAY CE 3.0 MODULE FOR PLUM A+ INFUSION SYSTEM UPGRADE
K141789 · Hospira, Inc. · Jan 2015
HOSPIRA MEDNET MEDICATION MANAGEMENT SUITE
K141102 · Hospira, Inc. · Jul 2014
BAXTER SIGMA SPECTRUM INFUSION PUMP WITH MASTER DRUG LIBRARY
K133801 · Baxter Healthcare Corporation · May 2014
CADD SOLIS VIP AMBULATORY INFUSION PUMP AND CADD SOLIS MEDICATION SAFETY SOFTWARE
K111275 · Smiths Medical Asd, Inc. · Feb 2013