PICOLAS NEODYMIUN-YAG OPHTHALMIC LASEER

FDA Premarket Approval P830080

Pre-market Approval Supplement Details

DevicePICOLAS NEODYMIUN-YAG OPHTHALMIC LASEER
Generic NameLaser, Neodymium:yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
ApplicantSYNEMED, INC.
Date Received1983-12-30
Decision Date1987-02-17
Notice Date1987-04-06
PMAP830080
SupplementS
Product CodeLOI 
Docket Number87M-0077
Advisory CommitteeOphthalmic
Expedited ReviewNo
Combination Product No
Applicant Address SYNEMED, INC. 1215 - 4th St. berkeley, CA 94710

Supplemental Filings

A PHP Error was encountered

Severity: Notice

Message: Undefined offset: 0

Filename: fda.report/pma_item.php

Line Number: 133

Backtrace:

File: /var/www/fda.report/pma_item.php
Line: 133
Function: _error_handler

Supplement NumberDateSupplement Type
P830080Original Filing

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