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

Radioimmunoassay, Total Estrogens In Pregnancy

21 CFR 862.1270 / Clinical Chemistry
FDA source (opens on fda.gov)

CHM is the FDA product code for Radioimmunoassay, Total Estrogens In Pregnancy, a class I device type, regulated under 21 CFR 862.1270. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
CHM
Device name
Radioimmunoassay, Total Estrogens In Pregnancy
Regulation
21 CFR 862.1270
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
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

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