Premarket Approval (PMA)

Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.

• Device: ND:YAG POSTERIOR CAPSULOTOMY MODEL 100
• Generic Name: Laser, neodymium:Yag, ophthalmic for uses other than posterior capsulotomy & cutting pupillary
• Applicant: NIDEK, INC.; 47651 WESTINGHOUSE DR.; FREMONT, CA 94539
• PMA Number: P830062
• Date Received: 01/25/1983
• Decision Date: 09/27/1984
• Withdrawal Date: 11/27/2013
• Product Code: LOI
• Docket Number: 84M-0353
• Notice Date: 11/26/1984
• Advisory Committee: Ophthalmic
• Expedited Review Granted?: No
• Combination Product: No
• Supplements: S001 S002 S006 S007 S009 S010 S011 S012 S014 S015 S016