FDA applicant

Daily Medical, Inc.

San Diego, CA1 decision1990–19900 recalls

FDA records 1 decision for Daily Medical, Inc. (San Diego, CA) in 1990: 1 510(k) clearance. All are in product code DWC (Controller, Temperature, Cardiopulmonary Bypass). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Daily Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Daily”

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

Daily Medical Products, Inc. 8

Daily Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Daily”