The following data is part of a premarket notification filed by Pro-dentec with the FDA for Vip Victor Interactive Probe.
Device ID | K960245 |
510k Number | K960245 |
Device Name: | VIP VICTOR INTERACTIVE PROBE |
Classification | Probe, Periodontic |
Applicant | PRO-DENTEC 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
Contact | Bob Zahradnik |
Correspondent | Bob Zahradnik PRO-DENTEC 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
Product Code | EIX |
CFR Regulation Number | 872.4565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-16 |
Decision Date | 1996-04-04 |
Summary: | summary |