HJC — Esthesiometer, Ocular Class I

FDA Device Classification

FDA product code HJC covers "Esthesiometer, Ocular", a Class I medical device regulated under 21 CFR 886.1040. Submissions are reviewed by the Ophthalmic panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HJC
Device Class
Class I
Regulation Number
886.1040
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K920271connecticut bioinstrumentsWEINSTEIN CORNEAL MIRCOAESTHESIOMETERApril 21, 1992
K851557luneauANESTHESIOMETERMay 30, 1985