FDA applicant

Patient Safety Products, Inc.

Brooklyn, NY1 decision1994–19940 recalls

FDA records 1 decision for Patient Safety Products, Inc. (Brooklyn, NY) in 1994: 1 510(k) clearance. All are in product code MMP (Cover, Barrier, Protective). 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, general and plastic surgery panel, where it files most

How often FDA has decided Patient Safety Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Patient Safety Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Patient Safety Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Patient”

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

Patient Solutions, Inc. 5 Patient Pocket, LLC 2 Patient Healthguards Corp. 1 Patient Data Systems 1

Patient Safety Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Patient”