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

Pump, Air, Non-Manual, For Endoscope

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

FEQ is the FDA product code for Pump, Air, Non-Manual, For Endoscope, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
FEQ
Device name
Pump, Air, Non-Manual, For Endoscope
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
21
Ingested recalls
5

Clearances, product code FEQ

By decision year
21 clearances under product code FEQ with a decision year between 2000 and 2022, 2010 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FEQ by decision year
YearClearances
20001
20091
20103
20111
20123
20131
20141
20152
20163
20171
20182
20191
20221

Applicants with the most clearances

Product code FEQ
Applicants holding the most 510(k) clearances under product code FEQ
ApplicantClearances
Boston Scientific Corporation6
United States Endoscopy Group, Inc.6
Erbe USA Inc3
KEYMED (Medical & Industrial Equipment) Ltd2
Byrne Medical, Inc.1
Keymed, Inc.1
STERIS Corporation1
United State Endoscopy Group, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 32 companies shown, in name order