Herpelisa Kit

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K822883 ↗

FDA Product Code

LGC

Device Class

Class II

Regulation

21 CFR Part 866.3305

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Chlamydelisa Test Kit

  Class I

  FDA 510(k) K821967 Active Cleared 3 Aug 1982

• Mycoplasmelisa Test Kit

  Class I

  FDA 510(k) K823804 Active Cleared 25 May 1983

• Cell Culture Reagents

  Class I

  FDA 510(k) K812531 Active Cleared 23 Oct 1981

• Cytomegelisa Test Kit

  Not classified

  FDA 510(k) K812123 Active Cleared 23 Sep 1981

• Measelisa Test Kit

  Class I

  FDA 510(k) K821762 Active Cleared 30 Jul 1982

• Digoxin Eia Kit

  Class II

  FDA 510(k) K801490 Active Cleared 14 Jul 1980

See all devices from M.A. Bioproducts →