510(k) Report

FDA applicant

Intelligent Medicine, Inc.

Denver, CO4 decisions1986–19860 recalls

FDA records 4 decisions for Intelligent Medicine, Inc. (Denver, CO) in 1986: 4 510(k) clearances. All are in product code FRN (Pump, Infusion). 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 Intelligent Medicine, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intelligent Medicine, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intelligent Medicine, 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 “Intelligent”

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