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

Column, Adsorption, Low Density, Lipoprotein

Unknown
FDA source (opens on fda.gov)

LXW is the FDA product code for Column, Adsorption, Low Density, Lipoprotein, a class III device type. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LXW
Device name
Column, Adsorption, Low Density, Lipoprotein
Device class
Class III
Review panel
Unknown
Submission type
Contact ODE
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LXW

By decision year
1 clearance under product code LXW with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LXW by decision year
YearClearances
19901

Applicants with the most clearances

Product code LXW
Applicants holding the most 510(k) clearances under product code LXW
ApplicantClearances
Baltimore Therapeutic Equipment Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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