FDA applicant

Mercury Enterprizes Dba Mercury Medical

Clearwater, FL1 decision2009–20090 recalls

FDA records 1 decision for Mercury Enterprizes Dba Mercury Medical (Clearwater, FL) in 2009: 1 510(k) clearance. All are in product code BYE (Attachment, Breathing, Positive End Expiratory…). 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, anesthesiology panel, where it files most

How often FDA has decided Mercury Enterprizes Dba Mercury Medical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Mercury Enterprizes Dba Mercury Medical by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mercury Enterprizes Dba Mercury Medical’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Mercury”

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

Mercury Medical 16 Mercury Enterprises, Inc. 3 Mercury Computer Systems, Inc. 2 Mercury Ent., Inc. D/B/A Mercury Medical 1 Mercury Electronics (Scot), Ltd. 1

Mercury Enterprizes Dba Mercury Medical

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Mercury”