A101 Litessager

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K914830 ↗

FDA Product Code

IRO

Device Class

Class I

Regulation

21 CFR Part 890.5975

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• F383 Rechargeable Mini Massager

  Class I

  FDA 510(k) K914703 Active Cleared 9 Dec 1991

• A013 Femi-Form Facial Massager

  Class I

  FDA 510(k) K931637 Active Cleared 28 Mar 1994

• FO51/F151 Golf Massager

  Class I

  FDA 510(k) K914706 Active Cleared 9 Dec 1991

• FO92 Seating Massager

  Class I

  FDA 510(k) K914829 Active Cleared 9 Dec 1991

• F055 B.O. Fantastic Relaxer

  Class I

  FDA 510(k) K914707 Active Cleared 9 Dec 1991

• FO41 Body Massager

  Class I

  FDA 510(k) K914705 Active Cleared 9 Dec 1991

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