510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K904743Substantially Equivalent

Lsi System II

M.S.P., Ltd., Overland Park KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904743 is the FDA 510(k) clearance record for LSI SYSTEM II, a class II device, cleared for M.S.P. , Ltd. on under FDA product code LIH (Interferential Current Therapy). FDA records list one 510(k) clearance for M.S.P. , Ltd. As of , FDA records show no recalls naming K904743.

Clearance record

Decision date
Received
(321 days to decision)
Product code
LIH Interferential Current Therapy
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
M.S.P. , Ltd. 8851 Bond, Overland Park KS
Third party review
No

Clearances, product code LIH

Trailing 12 months

FDA records hold no clearances under product code LIH in the trailing twelve months.

FDA records show no clearances under product code LIH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LIH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260