FDA applicant

Pressure Products, Inc.

Rancho Palos Verdes, CA1 decision1998–19980 recalls

FDA records 1 decision for Pressure Products, Inc. (Rancho Palos Verdes, CA) in 1998: 1 510(k) clearance. All are in product code DXC (Clamp, Vascular). 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 Pressure Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pressure Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pressure 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 “Pressure”

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

Pressure Products Medical Device Manufacturing, LLC 9 Pressure-Tech, Inc. 1 Pressure Point, Inc. 1

Pressure Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pressure”