FDA applicant

Timeter Instrument Corp.

Mchenry, IL29 decisions1976–19880 recalls

FDA records 29 decisions for Timeter Instrument Corp. (Mchenry, IL) from 1976 to 1988: 29 510(k) clearances. Most are in product codes CAX (Flowmeter, Tube, Thorpe, Back-Pressure…) and BYX (Tubing, Pressure And Accessories). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Timeter Instrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Timeter Instrument 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 “Timeter”

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

The Timeter Group 4

Timeter Instrument Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Timeter”