FDA applicant

Lifewatch Systems, Inc.

Attleboro, MA3 decisions1986–19870 recalls

FDA records 3 decisions for Lifewatch Systems, Inc. (Attleboro, MA) from 1986 to 1987: 3 510(k) clearances. All are in product code BZQ (Monitor, Breathing Frequency). 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 Lifewatch Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifewatch Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lifewatch”

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

Lifewatch Technologies, Ltd. 4 Lifewatch Services, Inc. 1

Lifewatch Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lifewatch”