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

Filiform And Filiform Follower

21 CFR 876.5520 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FBW is the FDA product code for Filiform And Filiform Follower, a class I device type, regulated under 21 CFR 876.5520. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FBW
Device name
Filiform And Filiform Follower
Regulation
21 CFR 876.5520
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
1
Ingested recalls
0

Clearances, product code FBW

By decision year
1 clearance under product code FBW with a decision year between 1991 and 1991, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FBW by decision year
YearClearances
19911

Applicants with the most clearances

Product code FBW
Applicants holding the most 510(k) clearances under product code FBW
ApplicantClearances
Baxter Healthcare Corporation1

Companies listing this code with FDA

Companies whose registered establishments list this code