Adult Incontinence Pad

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K834295 ↗

FDA Product Code

EYQ

Device Class

Class I

Regulation

21 CFR Part 876.5920

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Rely Tampon

  Class II

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• Unscented Menstrual Pad

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• Tampax Compak Pearl Plastic Applicator Scented and Unscented Tampons

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• Always Super Maxipad-Scented

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• Always Menstrual Pads

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  FDA 510(k) K071827 Active Cleared 20 Sep 2007

• Tampax Tampons (Junior, Regular, Super and Super Plus Absorbencies)

  Class II

  FDA 510(k) K040999 Active Cleared 9 Jul 2004

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