The following data is part of a premarket notification filed by Pac-dent International, Inc. with the FDA for Pacendo Sodium Hyprochlorite.
Device ID | K151852 |
510k Number | K151852 |
Device Name: | PacEndo Sodium Hyprochlorite |
Classification | Cleanser, Root Canal |
Applicant | PAC-DENT INTERNATIONAL, INC. 670 ENDEAVOR CIRCLE Brea, CA 92821 |
Contact | Wenying Zhu |
Correspondent | Wenying Zhu PAC-DENT INTERNATIONAL, INC. 670 ENDEAVOR CIRCLE Brea, CA 92821 |
Product Code | KJJ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-07-07 |
Decision Date | 2015-11-10 |
Summary: | summary |