510(k) Report

FDA applicant

Eastern Laboratories, Ltd.

Flushing, NY2 decisions1988–19890 recalls

FDA records 2 decisions for Eastern Laboratories, Ltd. (Flushing, NY) from 1988 to 1989: 2 510(k) clearances. All are in product code DIF (Drug Mixture Control Materials). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical toxicology panel, where it files most

How often FDA has decided Eastern Laboratories, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eastern Laboratories, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eastern Laboratories, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Eastern”

FDA records each applicant name separately; these may or may not be the same firm.