The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Dentastic One-step.
Device ID | K953301 |
510k Number | K953301 |
Device Name: | DENTASTIC ONE-STEP |
Classification | Cement, Dental |
Applicant | PULPDENT CORP. 80 OAKLAND ST. P.O. BOX 780 Watertown, MA 02471 -0780 |
Contact | Kenneth J Berk |
Correspondent | Kenneth J Berk PULPDENT CORP. 80 OAKLAND ST. P.O. BOX 780 Watertown, MA 02471 -0780 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-14 |
Decision Date | 1995-08-25 |