FDA applicant

Pari Holding Co.

Richmond, VA8 decisions1994–20010 recalls

FDA records 8 decisions for Pari Holding Co. (Richmond, VA) from 1994 to 2001: 8 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BWF (Spirometer, Therapeutic (Incentive)). 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 Pari Holding Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pari Holding Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pari”

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

Pari Respiratory Equipment, Inc. 10 Pari Innovative Manufacturers, Inc. 10

Pari Holding Co.

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 “Pari”