FDA applicant

Keller Medical Specialties Products, Inc.

Antioch, IL6 decisions1990–19990 recalls

FDA records 6 decisions for Keller Medical Specialties Products, Inc. (Antioch, IL) from 1990 to 1999: 6 510(k) clearances. Most are in product codes DQA (Oximeter) and DSJ (Alarm, Blood-Pressure). Its devices cite 4 predicates, 3 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 Keller Medical Specialties Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Keller Medical Specialties Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Keller Medical Specialties Products…’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 “Keller”

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

Keller Instruments, Inc. 5

Keller Medical Specialties Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Keller”