FDA applicant

Daily Medical Products, Inc.

San Diego, CA8 decisions1990–19920 recalls

FDA records 8 decisions for Daily Medical Products, Inc. (San Diego, CA) from 1990 to 1992: 8 510(k) clearances. Most are in product codes DWC (Controller, Temperature, Cardiopulmonary Bypass) and FLL (Continuous Measurement Thermometer). 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 Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Daily Medical Products, 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, Inc. 1

Daily Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Daily”