FDA applicant

Monitor Science Corp.

Mchenry, IL6 decisions1977–19790 recalls

FDA records 6 decisions for Monitor Science Corp. (Mchenry, IL) from 1977 to 1979: 6 510(k) clearances. Most are in product codes JFH (Acid Phosphatase (Prostatic), Tartrate Inhibited) and KLP (Amikacin Serum Assay). 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, clinical toxicology panel, where it files most

How often FDA has decided Monitor Science Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Monitor Science Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Monitor”

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

Monitor Instruments, Inc. 2 The Monitor Corp. 1 Monitor Mask, Inc. 1 Monitor/Demlar 1

Monitor Science Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Monitor”