FDA applicant

Ausam Biotecthnologies, Inc.

New York, NY1 decision2003–20030 recalls

FDA records 1 decision for Ausam Biotecthnologies, Inc. (New York, NY) in 2003: 1 510(k) clearance. All are in product code JIQ (Turbidimetric Method, Protein Or Albumin…). 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 chemistry panel, where it files most

How often FDA has decided Ausam Biotecthnologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ausam Biotecthnologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ausam Biotecthnologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?