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

Device, Vein Stabilization

21 CFR 880.6980 / General Hospital
FDA source (opens on fda.gov)

LBJ is the FDA product code for Device, Vein Stabilization, a class I device type, regulated under 21 CFR 880.6980. As of , FDA records hold no 510(k) clearances under this code and 6 recalls.

Classification record

Product code
LBJ
Device name
Device, Vein Stabilization
Regulation
21 CFR 880.6980
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
0
Ingested recalls
6

Companies listing this code with FDA

Companies whose registered establishments list this code