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

Die, Wire Bending, Ent, Sterile

21 CFR 874.3540 / Ear, Nose, Throat
FDA source (opens on fda.gov)

JXW is the FDA product code for Die, Wire Bending, Ent, Sterile, a class I device type, regulated under 21 CFR 874.3540. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
JXW
Device name
Die, Wire Bending, Ent, Sterile
Regulation
21 CFR 874.3540
Device class
Class I
Review panel
Ear, Nose, Throat
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
0

Companies listing this code with FDA

Companies whose registered establishments list this code