510(k) Report

FDA applicant

Medical Support Products, Inc.

Lancaster, PA1 decision1990–19900 recalls

FDA records 1 decision for Medical Support Products, Inc. (Lancaster, PA) in 1990: 1 510(k) clearance. All are in product code BXR (Meter, Airway Pressure (Inspiratory Force)). 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 Medical Support Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Support Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Support Products, Inc.’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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