The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Canal King (thin) Canal King (thick).
Device ID | K940368 |
510k Number | K940368 |
Device Name: | CANAL KING (THIN) CANAL KING (THICK) |
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 | 1994-01-26 |
Decision Date | 1995-01-20 |