FDA applicant

Taylor Instrument Analytics Co.

Mchenry, IL2 decisions1977–19780 recalls

FDA records 2 decisions for Taylor Instrument Analytics Co. (Mchenry, IL) from 1977 to 1978: 2 510(k) clearances. Most are in product codes KYT (Light, Examination, Medical, Battery Powered) and CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). 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 Taylor Instrument Analytics Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Taylor Instrument Analytics Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Taylor Instrument Analytics Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Taylor Instrument Analytics Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Taylor”

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

Taylor Medical Equipment 2 Taylor Industries, Inc. 2 Taylor Bio-Medical, Inc. 1 Taylor Corp. 1 Taylor H. Haynes, M.D. 1 Taylor Catheter Holder Mfg. 1 Taylor/Fox Enterprises, LLC 1

Taylor Instrument Analytics Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Taylor”