FDA applicant

Alternative Design Systems, Inc.

Carlstadt, NJ6 decisions1983–19880 recalls

FDA records 6 decisions for Alternative Design Systems, Inc. (Carlstadt, NJ) from 1983 to 1988: 6 510(k) clearances. Most are in product codes FLS (Monitor, Apnea, Facility Use) and LDD (Dc-Defibrillator, Low-Energy, (Including…). 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 Alternative Design Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alternative Design Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alternative Design 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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Other applicant names beginning “Alternative”

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

Alternative Pioneering Research and Development 2

Alternative Design Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Alternative”