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
FBPClass II

Telescope, Rigid, Endoscopic

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

FBP is the FDA product code for Telescope, Rigid, Endoscopic, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FBP
Device name
Telescope, Rigid, Endoscopic
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
5
Ingested recalls
0

Clearances, product code FBP

By decision year
5 clearances under product code FBP with a decision year between 1976 and 2015, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FBP by decision year
YearClearances
19761
19991
20031
20121
20151

Applicants with the most clearances

Product code FBP
Applicants holding the most 510(k) clearances under product code FBP
ApplicantClearances
Acmi Corporation1
Endoservice Optical Instruments GmbH1
Olympus Winter & Ibe GmbH1
Richard Wolf Medical Instruments Corp.1
V. Mueller O.V. Baxter Healthcare Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code