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

System, Alarm, Electrosurgical

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

FFI is the FDA product code for System, Alarm, Electrosurgical, a class II device type, regulated under 21 CFR 876.4300. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FFI
Device name
System, Alarm, Electrosurgical
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
1
Ingested recalls
0

Clearances, product code FFI

By decision year
1 clearance under product code FFI with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FFI by decision year
YearClearances
19841

Applicants with the most clearances

Product code FFI
Applicants holding the most 510(k) clearances under product code FFI
ApplicantClearances
Akron City Hospital1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code FFI.