3M Remover Lotion Product Number 86XX

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K925618 ↗

FDA Product Code

KOX

Device Class

Class I

Regulation

21 CFR Part 878.4730

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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  Class II

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  Class II

  FDA 510(k) K930681 Active Cleared 10 Feb 1994

• 3M Precise Brand Internal Surgical Staples

  Class II

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  Class II

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• 3M X-Large Sheet #7979/ #7979NS

  Class II

  FDA 510(k) K946025 Active Cleared 2 Feb 1995

• Red Dot 2515 Cardiac Sensor System

  Class I

  FDA 510(k) K924487 Active Cleared 23 Dec 1992

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