510(k) Report

FDA applicant

Life Measurement Instruments, Inc.

Davis, CA1 decision1995–19950 recalls

FDA records 1 decision for Life Measurement Instruments, Inc. (Davis, CA) in 1995: 1 510(k) clearance. All are in product code OAC (Plethysmograph, Air Displacement For Body…). 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, cardiovascular panel, where it files most

How often FDA has decided Life Measurement Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Life Measurement Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Life Measurement Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Life Measurement Instruments, Inc.’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

Which product codes does it file in?

  • OACPlethysmograph, Air Displacement For Body Composition Analysis1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K924972Sonamet Body Composition AnalyzerLife Measurement Instruments, Inc. · 19952cite it

What has FDA decided for it lately?

  • K924972Sonamet Body Composition AnalyzerLife Measurement Instruments, Inc. · 1995

The one decision as Life Measurement Instruments, Inc. →