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

Attachment, Teaching, For Endoscope

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

FEA is the FDA product code for Attachment, Teaching, For Endoscope, a class I 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
FEA
Device name
Attachment, Teaching, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FEA

By decision year
2 clearances under product code FEA with a decision year between 1979 and 1994, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FEA by decision year
YearClearances
19791
19941

Applicants with the most clearances

Product code FEA
Applicants holding the most 510(k) clearances under product code FEA
ApplicantClearances
American Optical Corp.1
JEDMED Instrument Company1

Companies listing this code with FDA

Companies whose registered establishments list this code