Healthcheck Digital Thermometer Model 1 Th-2

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K851379 ↗

FDA Product Code

FLL

Device Class

Class II

Regulation

21 CFR Part 880.2910

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Tenstar

  Class II

  FDA 510(k) K874818 Active Cleared 28 Sep 1988

• Healthcheck Auto Inflate Digital Bp Monitor Bp-2

  Class II

  FDA 510(k) K850070 Active Cleared 22 Jan 1985

• Digital Blood Pressure Monitor Model Cx-1

  Class II

  FDA 510(k) K881003 Active Cleared 18 May 1988

• Pulsonic Digital Blood Pressure Monitor Model BP-3

  Class II

  FDA 510(k) K860287 Active Cleared 28 Apr 1986

• Ptk Plus. Home Pregnancy Test

  Class II

  FDA 510(k) K861946 Active Cleared 16 Jun 1986

• C&T Pregnancy Test Kit

  Class II

  FDA 510(k) K884489 Active Cleared 8 Mar 1989

See all devices from Healthcheck Corp. →