HMD — Chair, Ophthalmic, Manual Class I

FDA Device Classification

FDA product code HMD covers "Chair, Ophthalmic, Manual", a Class I medical device regulated under 21 CFR 886.1140. 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
HMD
Device Class
Class I
Regulation Number
886.1140
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K833538vision health technologyDOWING OPHTHALMIC CHAIR-NON/AC POWERMarch 5, 1984