KYH — Endoscope, Ophthalmic Class II

FDA Device Classification

FDA product code KYH covers "Endoscope, Ophthalmic", a Class II medical device regulated under 21 CFR 876.1500. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KYH
Device Class
Class II
Regulation Number
876.1500
Submission Type
Review Panel
OP
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K941660gm engineeringGM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHTMay 24, 1994