FDA applicant

Dawn Medical

San Francisco, CA4 decisions1991–19940 recalls

FDA records 4 decisions for Dawn Medical (San Francisco, CA) from 1991 to 1994: 4 510(k) clearances. Most are in product codes BZG (Spirometer, Diagnostic) and GCY (Apparatus, Suction, Single Patient Use…). 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 Dawn Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dawn Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dawn”

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

Dawn of Hope Development Center 1 Dawn Laser Technology, Inc. 1

Dawn Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dawn”