510(k) Report

FDA applicant

Aerotel Medical Systems (1998), Ltd.

Hasbrouck Heights, NJ7 decisions1999–20030 recalls

FDA records 7 decisions for Aerotel Medical Systems (1998), Ltd. (Hasbrouck Heights, NJ) from 1999 to 2003: 7 510(k) clearances. Most are in product codes DXH (Transmitters And Receivers…) and DXN (System, Measurement, Blood-Pressure…). Its devices cite 8 predicates, 4 of them its own earlier devices. 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 Aerotel Medical Systems (1998), Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aerotel Medical Systems (1998), Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aerotel Medical Systems (1998), Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Aerotel Medical Systems (1998), Ltd.’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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Other applicant names beginning “Aerotel”

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