510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K022453Substantially Equivalent

Modification to Acuity Central Monitoring System

Welch Allyn Protocol, Inc., Beaverton OR / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K022453 is the FDA 510(k) clearance record for MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM, a class II device, cleared for Welch Allyn Protocol, Inc. on under FDA product code DSI (Detector And Alarm, Arrhythmia). FDA records list 7 510(k) clearances for Welch Allyn Protocol, Inc., from to . As of , FDA records show one recall naming K022453.

Clearance record

Decision date
Received
(26 days to decision)
Product code
DSI Detector And Alarm, Arrhythmia
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Welch Allyn Protocol, Inc. 8500 SW Creekside Pl., Beaverton OR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DSI

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