FDA applicant

Piper Medical Products

West Sacramento, CA3 decisions1998–19990 recalls

FDA records 3 decisions for Piper Medical Products (West Sacramento, CA) from 1998 to 1999: 3 510(k) clearances. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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 Piper Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Piper Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Piper Medical Products’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 “Piper”

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

Piper Access, LLC 3

Piper Medical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Piper”