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

Copper Reduction, Glucose

21 CFR 862.1345 / Clinical Chemistry
FDA source (opens on fda.gov)

CFW is the FDA product code for Copper Reduction, Glucose, a class II device type, regulated under 21 CFR 862.1345. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
CFW
Device name
Copper Reduction, Glucose
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code