The following data is part of a premarket notification filed by Kuraray Medical Inc. with the FDA for Clearfil Photo Core.
Device ID | K012705 |
510k Number | K012705 |
Device Name: | CLEARFIL PHOTO CORE |
Classification | Material, Tooth Shade, Resin |
Applicant | KURARAY MEDICAL INC. 30TH FL. METLIFE BUILDING 200 PARK AVENUE New York, NY 10166 |
Contact | Masaya Sasaki |
Correspondent | Masaya Sasaki KURARAY MEDICAL INC. 30TH FL. METLIFE BUILDING 200 PARK AVENUE New York, NY 10166 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-08-14 |
Decision Date | 2001-09-11 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
EKUR000356KA1 | K012705 | 000 |
EKUR000355KA1 | K012705 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLEARFIL PHOTO CORE 79009241 3171655 Live/Registered |
KURARAY CO., LTD. 2004-11-19 |