Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K112650Substantially Equivalent

Connexall Suite of Software Products

Connexall USA, Inc., Nederland CO / Traditional, Substantially Equivalent

K112650 is the FDA 510(k) clearance record for CONNEXALL SUITE OF SOFTWARE PRODUCTS, a class II device, cleared for Connexall USA, Inc. on under FDA product code MSX (System, Network And Communication, Physiological Monitors). FDA records list one 510(k) clearance for Connexall USA, Inc. As of , FDA records show no recalls naming K112650.

Clearance record

Decision date
Received
(142 days to decision)
Product code
MSX System, Network And Communication, Physiological Monitors
Regulation
21 CFR 870.2300
Device class
Class II
Review panel
Cardiovascular
Applicant
Connexall USA, Inc. P.O. Box 3018, Nederland CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MSX

Trailing 12 months
4 clearances under product code MSX in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MSX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20261
August 20261
September 20261
October 20260