FDA applicant

The Timeter Group

Lancaster, PA4 decisions1985–19870 recalls

FDA records 4 decisions for The Timeter Group (Lancaster, PA) from 1985 to 1987: 4 510(k) clearances. Most are in product codes CAN (Regulator, Pressure, Gas Cylinder) and KFZ (Humidifier, Non-Direct Patient Interface…). 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 The Timeter Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Timeter Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “The”

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

Timeter Instrument Corp. 29

The Timeter Group

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “The”