510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K151672Substantially Equivalent

Cerner CareAware Event Management

Cerner Corporation, Kansas City MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K151672 is the FDA 510(k) clearance record for Cerner CareAware Event Management, a class II device, cleared for Cerner Corporation on under FDA product code MSX (System, Network And Communication, Physiological Monitors). FDA records list 8 510(k) clearances for Cerner Corporation, from to . As of , FDA records show no recalls naming K151672.

Clearance record

Decision date
Received
(182 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
Cerner Corporation 2800 Rockcreek Pkwy., Kansas City MO
510(k) summary
Statement
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