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

Sigmoidoscope, Rigid, Electrical

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FAN is the FDA product code for Sigmoidoscope, Rigid, Electrical, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FAN
Device name
Sigmoidoscope, Rigid, Electrical
Regulation
21 CFR 876.1500
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
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FAN

By decision year
2 clearances under product code FAN with a decision year between 1983 and 2023, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FAN by decision year
YearClearances
19831
20231

Applicants with the most clearances

Product code FAN
Applicants holding the most 510(k) clearances under product code FAN
ApplicantClearances
C.R. Bard Inc1
Surgease Innovations Ltd1

Companies listing this code with FDA

Companies whose registered establishments list this code