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

Catheter And Tube, Suprapubic

21 CFR 876.5090 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FEZ is the FDA product code for Catheter And Tube, Suprapubic, a class II device type, regulated under 21 CFR 876.5090. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 2 recalls.

Classification record

Product code
FEZ
Device name
Catheter And Tube, Suprapubic
Regulation
21 CFR 876.5090
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
2

Clearances, product code FEZ

By decision year
1 clearance under product code FEZ with a decision year between 1977 and 1977, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FEZ by decision year
YearClearances
19771

Applicants with the most clearances

Product code FEZ
Applicants holding the most 510(k) clearances under product code FEZ
ApplicantClearances
Mentor1

Companies listing this code with FDA

Companies whose registered establishments list this code