GBP — Catheter, Multiple Lumen Class I

FDA Device Classification

FDA product code GBP covers "Catheter, Multiple Lumen", a Class I medical device regulated under 21 CFR 878.4200. Submissions are reviewed by the General, Plastic Surgery panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GBP
Device Class
Class I
Regulation Number
878.4200
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K844889goosen enterprisesMENSINK-GOOSEN CATHETERMarch 18, 1985
K821220clincal instrumentsMULTILUMEN INTRAVENOUS INFUSION CATHETERJuly 9, 1982
K820446dlpCATHETER, MULTIPLE LUMENMarch 11, 1982