510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K010453Substantially Equivalent

M2376a Devicelink System

Agilent Technologies, Inc., Andover MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K010453 is the FDA 510(k) clearance record for M2376A DEVICELINK SYSTEM, a class II device, cleared for Agilent Technologies, Inc. on under FDA product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)). FDA records list 51 510(k) clearances for Agilent Technologies, Inc., from to . As of , FDA records show no recalls naming K010453.

Clearance record

Decision date
Received
(15 days to decision)
Product code
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation
21 CFR 870.2300
Device class
Class II
Review panel
Cardiovascular
Applicant
Agilent Technologies, Inc. 3000 Minuteman Rd., Andover MA
510(k) summary
Summary
Third party review
No

Clearances, product code MWI

Trailing 12 months
5 clearances under product code MWI in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MWI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20262
September 20260
October 20260