FDA Device Intelligence
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Chamber, Patient Isolation

FDA product code LGM · Class 2 · General Hospital

9
Registered devices
3
Adverse events
1
Recalls
12
510(k) clearances

Devices with this code

Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.Carecube ISTARI — Carecubes, Inc.

Recent recalls

DateFirmReason
2014-06-27Life Force of Tampa, LLCThe Life Force chamber is marketed and promoted as a medical device, intended for use in the diagnosis of disease or other conditions or in the cure, mitigation

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.