Biosign Biological Indicator (Eight Month Exp.)

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

510(k) Number

K891366 ↗

FDA Product Code

FRC

Device Class

Class II

Regulation

21 CFR Part 880.2800

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Mdt Urology Table

  Class II

  FDA 510(k) K942485 Active Cleared 26 Aug 1994

• Spor-O-Therm

  Class I

  FDA 510(k) K801462 Active Cleared 28 Jul 1980

• Odontoson 3

  Class II

  FDA 510(k) K782133 Active Cleared 27 Feb 1979

• Stearothermohilus Spore Strips

  Class II

  FDA 510(k) K800482 Active Cleared 16 Apr 1980

• Mdt/Harvey Model 7000 & 8000 Chemiclave

  Class II

  FDA 510(k) K924380 Active Cleared 16 Feb 1994

• Mdt Dental Chair

  Class I

  FDA 510(k) K931169 Active Cleared 20 May 1993

See all devices from Mdt Corp., Inc. →