510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K901890Substantially Equivalent

Mark IV Floatation Therapy Bed

Hydrothermic Floatation Systems, Inc., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901890 is the FDA 510(k) clearance record for MARK IV FLOATATION THERAPY BED, a class II device, cleared for Hydrothermic Floatation Systems, Inc. on under FDA product code IOQ (Bed, Flotation Therapy, Powered). FDA records list one 510(k) clearance for Hydrothermic Floatation Systems, Inc. As of , FDA records show no recalls naming K901890.

Clearance record

Decision date
Received
(11 days to decision)
Product code
IOQ Bed, Flotation Therapy, Powered
Regulation
21 CFR 890.5170
Device class
Class II
Review panel
Physical Medicine
Applicant
Hydrothermic Floatation Systems, Inc. 6404 Hollywood Blvd., Los Angeles CA
Third party review
No

Clearances, product code IOQ

Trailing 12 months

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

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