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

Radioimmunoassay, Cyclic Gmp

21 CFR 862.1230 / Clinical Chemistry
FDA source (opens on fda.gov)

CGT is the FDA product code for Radioimmunoassay, Cyclic Gmp, a class II device type, regulated under 21 CFR 862.1230. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
CGT
Device name
Radioimmunoassay, Cyclic Gmp
Regulation
21 CFR 862.1230
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