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

Monitor,Test,Hiv-1

Unknown
FDA source (opens on fda.gov)

MTL is the FDA product code for Monitor,Test,Hiv-1, a class III device type. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
MTL
Device name
Monitor,Test,Hiv-1
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
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code