510(k) Report

FDA applicant

Inrange Systems, Inc.

Altoona, PA2 decisions2007–20150 recalls

FDA records 2 decisions for Inrange Systems, Inc. (Altoona, PA) from 2007 to 2015: 1 510(k) clearance and 1 De Novo grant. All are in product code NZH (Medication Management System, Remote). 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 hospital panel, where it files most

How often FDA has decided Inrange Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007: 12015: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Inrange Systems, 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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