Titertek Microplate Incubator

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K812340 ↗

FDA Product Code

JTQ

Device Class

Class I

Regulation

21 CFR Part 866.2540

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Trypsin 1%

  Class I

  FDA 510(k) K771955 Active Cleared 22 Nov 1977

• Adenovirus-Group Fa Labelled (8-651 Rf)

  Class I

  FDA 510(k) K770807 Active Cleared 20 May 1977

• Enteric-Tek

  Class I

  FDA 510(k) K792058 Active Cleared 11 Jan 1980

• Titertek Microplate Washer S-12

  Class I

  FDA 510(k) K862066 Active Cleared 5 Jun 1986

• Neigon Jembec Plate with Anixomycin

  Class II

  FDA 510(k) K760693 Active Cleared 7 Oct 1976

• Gentamicin Sulfate Solution (50mg Gentamicin)

  Class I

  FDA 510(k) K861823 Active Cleared 20 May 1986

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