510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FGXClass I

Snare, Non-Electrical

21 CFR 876.4730 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FGX is the FDA product code for Snare, Non-Electrical, a class I device type, regulated under 21 CFR 876.4730. As of , FDA records hold no 510(k) clearances under this code and 47 recalls.

Classification record

Product code
FGX
Device name
Snare, Non-Electrical
Regulation
21 CFR 876.4730
Device class
Class I
Review panel
Gastroenterology, Urology
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
47

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 50 companies shown, in name order