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

Electrode, Flexible Suction Coagulator

21 CFR 876.4300 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FEH is the FDA product code for Electrode, Flexible Suction Coagulator, a class II device type, regulated under 21 CFR 876.4300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FEH
Device name
Electrode, Flexible Suction Coagulator
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code FEH

By decision year
3 clearances under product code FEH with a decision year between 1981 and 2013, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FEH by decision year
YearClearances
19811
20121
20131

Applicants with the most clearances

Product code FEH
Applicants holding the most 510(k) clearances under product code FEH
ApplicantClearances
Optim LLC2
American Cystocope Makers, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code