HNZ — Curette, Ophthalmic Class I

FDA Device Classification

FDA product code HNZ covers "Curette, Ophthalmic", a Class I medical device regulated under 21 CFR 886.4350. 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
HNZ
Device Class
Class I
Regulation Number
886.4350
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K870437lookLOOK CAPSULE POLISHERS/SCRAPERSFebruary 20, 1987
K841007premier dental productsOPHTHALMIC CURETTE-VARIOUSMay 9, 1984