HJQ — Stereoscope, Ac-Powered Class I

FDA Device Classification

FDA product code HJQ covers "Stereoscope, Ac-Powered", a Class I medical device regulated under 21 CFR 886.1870. Submissions are reviewed by the Ophthalmic panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
HJQ
Device Class
Class I
Regulation Number
886.1870
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K830625richard-allan medical indCYTO-STAINMarch 24, 1983