The following data is part of a premarket notification filed by New World Medical, Inc. with the FDA for Ahmed Glaucoma Valve Implant.
Device ID | K991072 |
510k Number | K991072 |
Device Name: | AHMED GLAUCOMA VALVE IMPLANT |
Classification | Implant, Eye Valve |
Applicant | NEW WORLD MEDICAL, INC. 10763 EDISON CT. Rancho Cucamonga, CA 91730 |
Contact | A.m. Ahmed |
Correspondent | A.m. Ahmed NEW WORLD MEDICAL, INC. 10763 EDISON CT. Rancho Cucamonga, CA 91730 |
Product Code | KYF |
CFR Regulation Number | 886.3920 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-03-31 |
Decision Date | 1999-07-13 |
Summary: | summary |