FDA applicant

Dsrv, Inc.

Clarkston, GA2 decisions2014–20140 recalls

FDA records 2 decisions for Dsrv, Inc. (Clarkston, GA) in 2014: 2 510(k) clearances. All are in product code GIR (Reagent, Russel Viper Venom). 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, hematology panel, where it files most

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

FDA decisions per year

2in 2014

2014high 2 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Dsrv, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dsrv, Inc.

Which product codes does it file in?

What has FDA decided for it lately?