PMA P970053S002
- Device
- NIDEK EC-5000 EXCIMER LASER SYSTEM
- Applicant
- Nidek Co., Ltd.
- PMA number
- P970053
- Supplement
- S002
- Product code
- LZS
- Decision date
- 2000-04-14
- Classification
- Excimer Laser System
- Generic name
- Excimer laser system
- Approval order statement
- INDICATIONS FOR USE OF THE NIDEK EC-5000 EXCIMER LASER SYSTEM.
- Summary
- <a href="http://www.accessdata.fda.gov/cdrh_docs/pdf/P970053S002B.pdf" target="_new">Summary of Safety and Effectiveness</a>
Current openFDA PMA Record#
- Device
- NIDEK EC-5000 EXCIMER LASER SYSTEM
- Applicant
- Nidek Co., Ltd.
- PMA number
- P970053
- Supplement
- S002
- Product code
- LZS
- Generic name
- Excimer laser system
- Decision date
- 2000-04-14
- Decision code
- APPR
- Date received
- 1999-04-19
- Supplement type
- Panel Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- INDICATIONS FOR USE OF THE NIDEK EC-5000 EXCIMER LASER SYSTEM.