The following data is part of a premarket notification filed by Dentsply Intl. with the FDA for Rct Gel Root Canal Therapy Gel.
Device ID | K972234 |
510k Number | K972234 |
Device Name: | RCT GEL ROOT CANAL THERAPY GEL |
Classification | Syringe, Periodontic, Endodontic, Irrigating |
Applicant | DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Contact | P. Jeffery Lehn |
Correspondent | P. Jeffery Lehn DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Product Code | EIC |
CFR Regulation Number | 872.4565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-16 |
Decision Date | 1997-06-30 |
Summary: | summary |