510(k) Report

FDA applicant

Life Measurement, Inc.

Concord, CA2 decisions2004–20060 recalls

FDA records 2 decisions for Life Measurement, Inc. (Concord, CA) from 2004 to 2006: 2 510(k) clearances. All are in product code OAC (Plethysmograph, Air Displacement For Body…). Its devices cite 4 predicates, 0 of them its own earlier devices. 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, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Life Measurement, 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 Analysis2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K060848Bod PodLife Measurement, Inc. · 2006
  • K032610Modified Sonamet Body Composition AnalyzerLife Measurement, Inc. · 2004

All 2 as Life Measurement, Inc. →