FDA applicant

Lifeguard Medical Products, Inc.

Indianapolis, IN12 decisions1981–20020 recalls

FDA records 12 decisions for Lifeguard Medical Products, Inc. (Indianapolis, IN) from 1981 to 2002: 12 510(k) clearances. Most are in product codes CAN (Regulator, Pressure, Gas Cylinder) and BTM (Ventilator, Emergency, Manual (Resuscitator)). 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 Lifeguard Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifeguard Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lifeguard Medical Products, 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 “Lifeguard”

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

The Lifeguard Store, Inc. 1

Lifeguard Medical Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Lifeguard”