Polystyrene Micro-Liter Plate-Birchtree

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K831984 ↗

FDA Product Code

DGO

Device Class

Class II

Regulation

21 CFR Part 866.5510

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

• Polystyrene Microtiter Plate Immuno-

  Class II

  FDA 510(k) K832344 Active Cleared 21 Nov 1983

• Allergen Immunosorbents Ip Specific E

  Not classified

  FDA 510(k) K831496 Active Cleared 8 Aug 1983

• Polystyrene Microtiter Well Immunosor

  Class II

  FDA 510(k) K832345 Active Cleared 25 Nov 1983

• Logipe a Data Reducsystem Ip Specific-

  Class II

  FDA 510(k) K831774 Active Cleared 18 Jul 1983

• Ip Specific G

  Class II

  FDA 510(k) K830005 Active Cleared 2 Jun 1983

• IP Specific E

  Class II

  FDA 510(k) K821094 Active Cleared 7 May 1982

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