Instrument Pad

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K791864 ↗

FDA Product Code

KKX

Device Class

Class II

Regulation

21 CFR Part 878.4370

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Rely Tampon

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• Unscented Menstrual Pad

  Class I

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

  Class II

  FDA 510(k) K040999 Active Cleared 9 Jul 2004

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