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

Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

Unknown
FDA source (opens on fda.gov)

LOK is the FDA product code for Kit, Test, Alpha-Fetoprotein For Neural Tube Defects, a class III device type. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
LOK
Device name
Kit, Test, Alpha-Fetoprotein For Neural Tube Defects
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code