HNW — Dilator, Lachrymal Class I

FDA Device Classification

FDA product code HNW covers "Dilator, Lachrymal", a Class I medical device regulated under 21 CFR 886.4350. Submissions are reviewed by the Ophthalmic panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HNW
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
K862070intermedics intraocularINTER-SHARPJune 17, 1986
K841002premier dental productsLACHRYMAL PROBES-VARIOUSMay 9, 1984
K812097koiKOI LACREMAL HOOK & DILATORAugust 18, 1981