Stockings, Rvs Tm

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

510(k) Number

K770466 ↗

FDA Product Code

EQL

Device Class

Class I

Regulation

21 CFR Part 874.4750

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Deseret Intravascular Catheter

  Class II

  FDA 510(k) K843033 Active Cleared 3 Dec 1984

• Deseret Neonatal Catheter Set

  Class II

  FDA 510(k) K834393 Active Cleared 13 Feb 1984

• Deseret Heparin Coated Flow Directed

  Class II

  FDA 510(k) K841317 Active Cleared 11 Jun 1984

• Orthopedic Tubular Stockinette

  Class I

  FDA 510(k) K760817 Active Cleared 20 Oct 1976

• Razor, Schick Disposable

  Not classified

  FDA 510(k) K760342 Active Cleared 11 Aug 1976

• Underpad, Disposable Polypropy. (Unilux)

  Class I

  FDA 510(k) K760164 Active Cleared 20 Jul 1976

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