510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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QLMNot classified

Intensive Care Unit, Respiratory Failure And Hemodynamic Instability Tool

Unknown
FDA source (opens on fda.gov)

QLM is the FDA product code for Intensive Care Unit, Respiratory Failure And Hemodynamic Instability Tool. FDA's definition for this code reads: "To be used by healthcare providers in the Intensive Care Unit (ICU) for adult patients for the computation of patient status indices as an adjunct to patient monitoring during the declared public health emergency". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QLM
Device name
Intensive Care Unit, Respiratory Failure And Hemodynamic Instability Tool
FDA definition
To be used by healthcare providers in the Intensive Care Unit (ICU) for adult patients for the computation of patient status indices as an adjunct to patient monitoring during the declared public health emergency.
Device class
Not classified
Review panel
Unknown
Submission type
FDA code 8
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code QLM.