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
GBPClass I

Catheter, Multiple Lumen

21 CFR 878.4200 / General, Plastic Surgery
FDA source (opens on fda.gov)

GBP is the FDA product code for Catheter, Multiple Lumen, a class I device type, regulated under 21 CFR 878.4200. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GBP
Device name
Catheter, Multiple Lumen
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code GBP

By decision year
3 clearances under product code GBP with a decision year between 1982 and 1985, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code GBP by decision year
YearClearances
19822
19851

Applicants with the most clearances

Product code GBP
Applicants holding the most 510(k) clearances under product code GBP
ApplicantClearances
Clincal Instruments Corp.1
Dlp, Inc.1
Goosen Enterprises, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order