The following data is part of a premarket notification filed by Jedental Co., Inc. with the FDA for Jedental Zinc Cement Improved.
Device ID | K933554 |
510k Number | K933554 |
Device Name: | JEDENTAL ZINC CEMENT IMPROVED |
Classification | Cement, Dental |
Applicant | JEDENTAL CO., INC. 324 SECOND ST. PIKE Southampton, PA 18966 |
Contact | John Wong |
Correspondent | John Wong JEDENTAL CO., INC. 324 SECOND ST. PIKE Southampton, PA 18966 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-07-21 |
Decision Date | 1993-11-01 |