The following data is part of a premarket notification filed by Satelec-acteon Group with the FDA for Proultra Piezo Ultrasonic.
Device ID | K113430 |
510k Number | K113430 |
Device Name: | PROULTRA PIEZO ULTRASONIC |
Classification | Scaler, Ultrasonic |
Applicant | SATELEC-ACTEON GROUP 124 GAITHER DRIVE , SUITE 140 Mt Laurel, NJ 08054 |
Contact | Rick Rosati |
Correspondent | Rick Rosati SATELEC-ACTEON GROUP 124 GAITHER DRIVE , SUITE 140 Mt Laurel, NJ 08054 |
Product Code | ELC |
CFR Regulation Number | 872.4850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-21 |
Decision Date | 2012-02-23 |