GCE — Adaptor, Catheter Class I

FDA Device Classification

FDA product code GCE covers "Adaptor, Catheter", a Class I medical device regulated under 21 CFR 878.4200. Submissions are reviewed by the General, Plastic Surgery panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GCE
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
K901716jeff klein surgicalKLEIN CONNECTOR(TM)May 11, 1990
K901715jeff klein surgicalKLEIN CORK(TM)May 11, 1990
K855039mediflex intlMEDIFLEX INJECTION CAPJanuary 24, 1986
K801680quintonBETA-CAP II ADAPTERAugust 4, 1980