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U.S. Department of Health and Human Services

Product Classification

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Device bath, sitz, powered
Regulation Description Immersion hydrobath.
Regulation Medical Specialty Physical Medicine
Review Panel Physical Medicine
Product CodeILM
Premarket Review Office of Device Evaluation (ODE)
Division of Neurological and Physical Medicine Devices (DNPMD)
Physical Medicine and Neurotherapueutic Devices Branch (PNDB)
Submission Type 510(K) Exempt
Regulation Number 890.5100
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
    Note: Class II devices the Food and Drug Administration (FDA) has also published a list of Class II (special controls) devices subject to certain limitations, that are now exempt from the premarket notification requirements under the Food and Drug Administration Modernization Act of 1997 (the Modernization Act). FDA believes that these exemptions will relieve manufacturers from the need to submit premarket notification submissions for these devices and will enable FDA to redirect the resources that would be spent on reviewing such submissions to more significant public health issues. FDA is taking this action in order to meet a requirement of the Modernization Act.
Guidance Document
  • Guidance Document for the Preparation of Premarket Notification [510(k)] Applications for Immersion Hydrobaths
Third Party Review
Accredited Persons

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