510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K861218Substantially Equivalent

Aqua Ark, Immersion Hydrobath

Aqua Ark, Inc., Allentown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861218 is the FDA 510(k) clearance record for AQUA ARK, IMMERSION HYDROBATH, a class II device, cleared for Aqua Ark, Inc. on under FDA product code ILJ (Bath, Hydro-Massage). FDA records list one 510(k) clearance for Aqua Ark, Inc. As of , FDA records show no recalls naming K861218.

Clearance record

Decision date
Received
(18 days to decision)
Product code
ILJ Bath, Hydro-Massage
Regulation
21 CFR 890.5100
Device class
Class II
Review panel
Physical Medicine
Applicant
Aqua Ark, Inc. C/O Commonwealth Med Corp Amer, Allentown PA
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