Ultraclone Ecl-01-800 Cell Line

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

510(k) Number

K841337 ↗

FDA Product Code

KIR

Device Class

Class I

Regulation

21 CFR Part 864.2280

Advisory Committee

Hematology

FDA Decision

SESE Substantially Equivalent

• Ultraclone Ecl-01-300 Cell Line

  Class I

  FDA 510(k) K841344 Active Cleared 11 May 1984

• Ultraclone Ecl-01-900 Cell Line

  Class I

  FDA 510(k) K843862 Active Cleared 17 Oct 1984

• Ultraclone Ecl-01-800 Cell Line

  Class I

  FDA 510(k) K851545 Active Cleared 10 May 1985

• Ultraclone Ecl-01-100 Cell Line

  Class I

  FDA 510(k) K841343 Active Cleared 11 May 1984

• Ultraclone Ecl-01-1400 Cell Line

  Class I

  FDA 510(k) K843864 Active Cleared 17 Oct 1984

• Ultraclone Ecl-01-2100 Cell Line

  Class I

  FDA 510(k) K843578 Active Cleared 31 Oct 1984

See all devices from Earl-Clay Laboratories, Inc. →