FDA applicant

Lifeline Instruments, Inc.

Mchenry, IL2 decisions1976–19810 recalls

FDA records 2 decisions for Lifeline Instruments, Inc. (Mchenry, IL) from 1976 to 1981: 2 510(k) clearances. All are in product code KSQ (Device, Blood Mixing And Blood Weighing). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Lifeline Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lifeline Instruments, 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 “Lifeline”

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

Lifeline Systems, Inc. 4 Lifeline Software, Inc. 3 Lifeline Medical Systems, Inc. 1 Lifeline Controls 1

Lifeline Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lifeline”