The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Pulpdent Seal-rite Udma.
Device ID | K963921 |
510k Number | K963921 |
Device Name: | PULPDENT SEAL-RITE UDMA |
Classification | Sealant, Pit And Fissure, And Conditioner |
Applicant | PULPDENT CORP. 80 OAKLAND ST. Watertown, MA 02472 |
Contact | Kenneth J Berk |
Correspondent | Kenneth J Berk PULPDENT CORP. 80 OAKLAND ST. Watertown, MA 02472 |
Product Code | EBC |
CFR Regulation Number | 872.3765 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-30 |
Decision Date | 1996-11-12 |
Summary: | summary |