510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FBMClass I

Cannula And Trocar, Suprapubic, Non-Disposable

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

FBM is the FDA product code for Cannula And Trocar, Suprapubic, Non-Disposable, a class I device type, regulated under 21 CFR 876.5090. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FBM
Device name
Cannula And Trocar, Suprapubic, Non-Disposable
Regulation
21 CFR 876.5090
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
9
Ingested recalls
0

Clearances, product code FBM

By decision year
9 clearances under product code FBM with a decision year between 1990 and 1996, 1990 the highest year at 6.
Show the numbers
510(k) clearances under FDA product code FBM by decision year
YearClearances
19906
19911
19941
19961

Applicants with the most clearances

Product code FBM
Applicants holding the most 510(k) clearances under product code FBM
ApplicantClearances
Solos Endoscopy, Inc.6
Core Dynamics, Inc.2
Snowden-Pencer1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 49 companies shown, in name order