Glass Mercury Filled Thermometers

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K893602 ↗

FDA Product Code

FLK

Device Class

Class II

Regulation

21 CFR Part 880.2920

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Opsite*wound (Flexigrid Application System)

  Class I

  FDA 510(k) K895408 Active Cleared 14 Dec 1989

• Allevyn Dressing Claims Change

  Class I

  FDA 510(k) K904412 Active Cleared 23 Oct 1990

• Solosite Dermal Wound Gel

  Unclassified

  FDA 510(k) K932263 Active Cleared 1 Oct 1993

• Allevyn Adhesive

  Class I

  FDA 510(k) K945330 Active Cleared 9 Feb 1995

• Cavi-Care Conforming Foam Dressing

  Class I

  FDA 510(k) K943619 Active Cleared 19 Aug 1994

• Allevyn Tracheostomy Dressing

  Class I

  FDA 510(k) K890748 Active Cleared 8 Mar 1989

See all devices from Smith & Nephew United, Inc. →