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

Recorder, External, Pressure, Amplifier & Transducer

21 CFR 876.1725 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FES is the FDA product code for Recorder, External, Pressure, Amplifier & Transducer, a class II device type, regulated under 21 CFR 876.1725. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FES
Device name
Recorder, External, Pressure, Amplifier & Transducer
Regulation
21 CFR 876.1725
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
2
Ingested recalls
0

Clearances, product code FES

By decision year
2 clearances under product code FES with a decision year between 1980 and 1989, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FES by decision year
YearClearances
19801
19891

Applicants with the most clearances

Product code FES
Applicants holding the most 510(k) clearances under product code FES
ApplicantClearances
Ferguson Medical1
Medical Measurements, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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