Lorrex Health Products - Clinical Mercury Thermome

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K923225 ↗

FDA Product Code

FLK

Device Class

Class II

Regulation

21 CFR Part 880.2920

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Super/Fluff Sponges

  Unclassified

  FDA 510(k) K942106 Active Cleared 19 May 1994

• Peanut Dissector

  Class I

  FDA 510(k) K945336 Active Cleared 5 Dec 1994

• Kittner Dissector

  Class I

  FDA 510(k) K945333 Active Cleared 28 Dec 1994

• Lorrex IV Sponges, Sterile 2'S; Lorrex Drain Sponges, Sterile 2'S

  Unclassified

  FDA 510(k) K942824 Active Cleared 3 Aug 1994

• Cherry Dissector

  Class I

  FDA 510(k) K945335 Active Cleared 28 Dec 1994

• Lorex Tracheostomy Gauze Sponges - Sterile 1'S and 2'S

  Unclassified

  FDA 510(k) K941955 Active Cleared 12 May 1994

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