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

Kit, Dna Detection, Human Papillomavirus

Unknown
FDA source (opens on fda.gov)

MAQ is the FDA product code for Kit, Dna Detection, Human Papillomavirus, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 12 recalls.

Classification record

Product code
MAQ
Device name
Kit, Dna Detection, Human Papillomavirus
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
12

Companies listing this code with FDA

Companies whose registered establishments list this code