-

510(k) Premarket Notification

Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA
 


New Search Back To Search Results
Device Classification Name weights, eyelid, external
510(k) NumberK011740
Device NameCONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)
Applicant
MEDDEV CORP.
730 north pastoria ave.
sunnyvale,  CA  94085
Contactsuzanna brick
Classification Product Code
MML  
Date Received06/05/2001
Decision Date 07/02/2001
Decision substantially equivalent (SE)
Classification Advisory Committee Ophthalmic
Review Advisory Committee Ophthalmic
Statement/Summary/Purged Status Summary only
summary summary
Type Special
Reviewed by Third Party No
Expedited Review No
 
-
-
-
-
-