The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Pulpdent Canal Finder.
Device ID | K945811 |
510k Number | K945811 |
Device Name: | PULPDENT CANAL FINDER |
Classification | Locator, Root Apex |
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 | LQY |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-28 |
Decision Date | 1995-01-20 |