510(k) Report

FDA applicant

Time Motion System Co.

Mchenry, IL2 decisions1978–19820 recalls

FDA records 2 decisions for Time Motion System Co. (Mchenry, IL) from 1978 to 1982: 2 510(k) clearances. All are in product code FFG (Device, Urine Flow Rate Measuring…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Time Motion System Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Time Motion System Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FFGDevice, Urine Flow Rate Measuring, Non-Electrical, Disposable1decision

What has FDA decided for it lately?

  • K820789Cancan 2002 Dental Patient ChairTime Motion System Co. · 1982
  • K781597PM 2000 Automatic Patient ChairTime Motion System Co. · 1978

All 2 as Time Motion System Co. →

Other applicant names beginning “Time”

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

Time Medical Limited 6Time Computer, Inc. (Tci) 1Time Medical Systems, Inc. 1Time IS Brain, S.L. 1