MICRORUPTOR MR-2 ND:YAG LASER SYSTEM

FDA Premarket Approval P840012 S002

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceMICRORUPTOR MR-2 ND:YAG LASER SYSTEM
Generic NameLaser, Neodymium:yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
ApplicantMERIDIAN AG
Date Received1987-03-26
Decision Date1987-06-22
PMAP840012
SupplementS002
Product CodeLOI 
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address MERIDIAN AG bierigutstrauss 7 ch-3608 thun, Be 

Supplemental Filings

Supplement NumberDateSupplement Type
P840012Original Filing
S007 1989-12-20 Normal 180 Day Track
S006 1989-12-07 Normal 180 Day Track
S005 1988-10-04 Normal 180 Day Track
S004
S003 1987-04-01 Panel Track
S002 1987-03-26 Normal 180 Day Track
S001 1986-01-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.