510(k) Report

FDA applicant

Body Composition Analog, Inc.

Schaumburg, IL2 decisions1987–19910 recalls

FDA records 2 decisions for Body Composition Analog, Inc. (Schaumburg, IL) from 1987 to 1991: 2 510(k) clearances. All are in product code DSB (Plethysmograph, Impedance). 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 Body Composition Analog, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Body Composition Analog, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Body Composition Analog, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Body”

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