510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K841954Substantially Equivalent

Oasis Club Hydromassage

Prexcor America, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K841954 is the FDA 510(k) clearance record for OASIS CLUB HYDROMASSAGE, a class II device, cleared for Prexcor America, Inc. on under FDA product code ILJ (Bath, Hydro-Massage). FDA records list one 510(k) clearance for Prexcor America, Inc. As of , FDA records show no recalls naming K841954.

Clearance record

Decision date
Received
(9 days to decision)
Product code
ILJ Bath, Hydro-Massage
Regulation
21 CFR 890.5100
Device class
Class II
Review panel
Physical Medicine
Applicant
Prexcor America, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ILJ

Trailing 12 months

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

FDA records show no clearances under product code ILJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ILJ, 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