Product code LOI— Unknown
NANOLAS ND:YAG OPHTHALMIC LASER
- Classification name
- Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
- Device class
- Class 3
- Advisory panel
- Unknown
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LOI
FDA has cleared device under product code LOI, all in 1988, filed by 1 applicant company. No FDA device recalls reference this product code. Class III devices are high-risk and generally require premarket approval (PMA); 510(k) clearance under a Class III product code is limited to certain preamendments-type devices.
Top applicants under product code LOI
Recent clearances under product code LOI
Data sourced from openFDA. This site is unofficial and independent of the FDA.