The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Pulpdent Edta Preparations.
Device ID | K932791 |
510k Number | K932791 |
Device Name: | PULPDENT EDTA PREPARATIONS |
Classification | Resin, Root Canal Filling |
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 | KIF |
CFR Regulation Number | 872.3820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-09 |
Decision Date | 1993-09-20 |