FDA applicant

Allied Fisher Scientific

Orangeburg, NY1 decision1985–19850 recalls

FDA records 1 decision for Allied Fisher Scientific (Orangeburg, NY) in 1985: 1 510(k) clearance. All are in product code GTQ (Antistreptolysin - Titer/Streptolysin O Reagent). 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, microbiology panel, where it files most

How often FDA has decided Allied Fisher Scientific’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allied Fisher Scientific since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Allied”

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

Allied Healthcare Products, Inc. 26 Allied Associates, Inc. 9 Allied Biomedical Corp. 9 Allied Instrumentation Laboratory 7 Allied Signal, Inc. 2 Allied Rubber Industries Sdn. Bhd. 2 Allied Photo Products Co., Inc. 1 Allied Hill Enterprises, Ltd. 1 Allied Dental Solutions 1 Allied Medical Technologies, Inc. 1 Allied Systems Co. 1 Allied Advanced Technologies (Aat) 1

Allied Fisher Scientific

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allied”