The following data is part of a premarket notification filed by Ultradent Products, Inc. with the FDA for File-eze.
Device ID | K934415 |
510k Number | K934415 |
Device Name: | FILE-EZE |
Classification | Cleanser, Root Canal |
Applicant | ULTRADENT PRODUCTS, INC. 2057 SUMMIT DR. Lake Oswego, OR 97034 |
Contact | Arthur J Saffir |
Correspondent | Arthur J Saffir ULTRADENT PRODUCTS, INC. 2057 SUMMIT DR. Lake Oswego, OR 97034 |
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 | 1993-09-10 |
Decision Date | 1994-04-13 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00883205106711 | K934415 | 000 |
00883205105431 | K934415 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FILE-EZE 74237678 1714978 Live/Registered |
Ultradent Products, Inc. 1992-01-14 |