510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K143057Substantially Equivalent

M3290B Philips IntelliVue Information Center iX

Philips North America LLC, Andover MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K143057 is the FDA 510(k) clearance record for M3290B Philips IntelliVue Information Center iX, a class II device, cleared for Philips Medical Systems on under FDA product code MSX (System, Network And Communication, Physiological Monitors). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show one recall naming K143057.

Clearance record

Decision date
Received
(40 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
Philips Medical Systems 3000 Minuteman Rd., Andover MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MSX

Trailing 12 months
5 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 20261