HRK — Table, Instrument, Manual, Ophthalmic Class I

FDA Device Classification

FDA product code HRK covers "Table, Instrument, Manual, Ophthalmic", a Class I medical device regulated under 21 CFR 886.4855. 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
HRK
Device Class
Class I
Regulation Number
886.4855
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842410american edwards laboratoriesAMER. EDWARDS LAB FLEXISCOPENovember 5, 1984
K760697alcon laboratoriesEVANS ARM AND HAND RESTNovember 2, 1976