ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

Laser, Neodymium:yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Premarket Approval P830062

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.

Pre-market Approval Supplement Details

DeviceND:YAG POSTERIOR CAPSULOTOMY MODEL 100
Classification NameLaser, Neodymium:yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
Generic NameLaser, Neodymium:yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
ApplicantNIDEK, INC.
Date Received1983-01-25
Decision Date1984-09-27
Notice Date1984-11-26
PMAP830062
SupplementS
Product CodeLOI
Docket Number84M-0353
Advisory CommitteeOphthalmic
Expedited ReviewNo
Combination Product No
Applicant Address NIDEK, INC. 47651 Westinghouse Dr. fremont, CA 94539

Supplemental Filings

Supplement NumberDateSupplement Type
P830062Original Filing
S016 1990-01-12 Normal 180 Day Track
S015 1989-08-08 Normal 180 Day Track
S014 1989-04-10 Normal 180 Day Track
S013
S012 1988-03-15 Normal 180 Day Track
S011 1987-03-23 Normal 180 Day Track
S010 1986-09-02 Normal 180 Day Track
S009 1986-03-19
S008
S007 1985-09-16
S006 1985-03-04
S005
S004
S003
S002 1984-10-15
S001 1984-07-12

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