FDA applicant

Kent Barker & Assoc.

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Kent Barker & Assoc. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code DRQ (Amplifier And Signal Conditioner, Transducer…). 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 Kent Barker & Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kent Barker & Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kent Barker & Assoc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Kent”

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

Kent Laboratories, Inc. 40 Kent Design & Manufacturing, Inc. 6 Kent Imaging, Inc. 5 Kent J. Toone, D.D.S. 1 Kent Medical Devices, Inc. 1

Kent Barker & Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kent”