HLS — Exophthalmometer Class I

FDA Device Classification

FDA product code HLS covers "Exophthalmometer", a Class I medical device regulated under 21 CFR 886.1270. 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
HLS
Device Class
Class I
Regulation Number
886.1270
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K771900welch allyn71110 DESK CHARGERNovember 9, 1977