LOI — Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary Class III

FDA Device Classification

FDA product code LOI covers "Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary", a Class III medical device. Submissions are reviewed by the Unknown panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
LOI
Device Class
Class III
Regulation Number
Submission Type
Review Panel
OP
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K881459biophysic medicalNANOLAS ND:YAG OPHTHALMIC LASERApril 13, 1988