The following data is part of a premarket notification filed by Premier Dental Products Co. with the FDA for Radiopaque, Glass Ionomer Endodontic Cement.
Device ID | K042215 |
510k Number | K042215 |
Device Name: | RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT |
Classification | Cement, Dental |
Applicant | PREMIER DENTAL PRODUCTS CO. 1710 ROMANO DR. Plymouth Meeting, PA 19462 |
Contact | Vince D'alessandro |
Correspondent | Vince D'alessandro PREMIER DENTAL PRODUCTS CO. 1710 ROMANO DR. Plymouth Meeting, PA 19462 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-16 |
Decision Date | 2004-09-21 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00887919552185 | K042215 | 000 |
00887919552178 | K042215 | 000 |