FDZ — Attachment, Eyepiece, For Insertion Of Prescription Lens Class I

FDA Device Classification

FDA product code FDZ covers "Attachment, Eyepiece, For Insertion Of Prescription Lens", a Class I medical device regulated under 21 CFR 876.1500. Submissions are reviewed by the Gastroenterology, Urology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
FDZ
Device Class
Class I
Regulation Number
876.1500
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K895772exel intlEXEL INDWELLING CATHETERFebruary 16, 1990
K852642teleflexmedicalCENTRAL VEIN CATHETERIZATION TRAYJanuary 16, 1986