The following data is part of a premarket notification filed by Southern Dental Industries, Inc. with the FDA for Riva Luting.
Device ID | K040393 |
510k Number | K040393 |
Device Name: | RIVA LUTING |
Classification | Cement, Dental |
Applicant | SOUTHERN DENTAL INDUSTRIES, INC. 729 N. ROUTE 83, SUITE 315 Bensenville, IL 60106 |
Contact | Samantha J Cheetham |
Correspondent | Samantha J Cheetham SOUTHERN DENTAL INDUSTRIES, INC. 729 N. ROUTE 83, SUITE 315 Bensenville, IL 60106 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-02-17 |
Decision Date | 2004-04-30 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
DO3686509001 | K040393 | 000 |
DO3686505101 | K040393 | 000 |
DO3686505081 | K040393 | 000 |
DO3686501081 | K040393 | 000 |
DO3686500081 | K040393 | 000 |