FDA applicant

Advanced Cytometrix, Inc.

Sunnyvale, CA3 decisions1995–19950 recalls

FDA records 3 decisions for Advanced Cytometrix, Inc. (Sunnyvale, CA) in 1995: 3 510(k) clearances. All are in product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Advanced Cytometrix, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Advanced Cytometrix, Inc.

Which product codes does it file in?

What has FDA decided for it lately?